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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Genome-Wide Scan for Linkage to Type 1 Diabetes in 2,496 Multiplex Families From the Type 1 Diabetes Genetics Consortium</title><author><name sortKey="Concannon, Patrick" sort="Concannon, Patrick" uniqKey="Concannon P" first="Patrick" last="Concannon">Patrick Concannon</name><affiliation><nlm:aff id="aff1">Department of Biochemistry and Molecular Genetics, University of Virginia, Charlottesville, Virginia;</nlm:aff></affiliation><affiliation><nlm:aff id="aff2">Center for Public Health Genomics, University of Virginia, Charlottesville, Virginia;</nlm:aff></affiliation></author><author><name sortKey="Chen, Wei Min" sort="Chen, Wei Min" uniqKey="Chen W" first="Wei-Min" last="Chen">Wei-Min Chen</name><affiliation><nlm:aff id="aff2">Center for Public Health Genomics, University of Virginia, Charlottesville, Virginia;</nlm:aff></affiliation><affiliation><nlm:aff id="aff3">Department of Public Health Sciences, Division of Biostatistics and Epidemiology, University of Virginia, Charlottesville, Virginia;</nlm:aff></affiliation></author><author><name sortKey="Julier, Cecile" sort="Julier, Cecile" uniqKey="Julier C" first="Cécile" last="Julier">Cécile Julier</name><affiliation><nlm:aff id="aff4">INSERM U730, Centre National de Génotypage, Evry, France;</nlm:aff></affiliation></author><author><name sortKey="Morahan, Grant" sort="Morahan, Grant" uniqKey="Morahan G" first="Grant" last="Morahan">Grant Morahan</name><affiliation><nlm:aff id="aff5">Centre for Diabetes Research, The Western Australian Institute for Medical Research and Centre for Medical Research, University of Western Australia, Perth, Australia;</nlm:aff></affiliation></author><author><name sortKey="Akolkar, Beena" sort="Akolkar, Beena" uniqKey="Akolkar B" first="Beena" last="Akolkar">Beena Akolkar</name><affiliation><nlm:aff id="aff6">Division of Diabetes, Endocrinology, and Metabolic Diseases, The National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland;</nlm:aff></affiliation></author><author><name sortKey="Erlich, Henry A" sort="Erlich, Henry A" uniqKey="Erlich H" first="Henry A." last="Erlich">Henry A. Erlich</name><affiliation><nlm:aff id="aff7">Roche Molecular Systems, Pleasanton, California;</nlm:aff></affiliation></author><author><name sortKey="Hilner, Joan E" sort="Hilner, Joan E" uniqKey="Hilner J" first="Joan E." last="Hilner">Joan E. Hilner</name><affiliation><nlm:aff id="aff8">Public Health Sciences, Wake Forest University School of Medicine, Winston-Salem, North Carolina;</nlm:aff></affiliation></author><author><name sortKey="Nerup, J Rn" sort="Nerup, J Rn" uniqKey="Nerup J" first="J Rn" last="Nerup">J Rn Nerup</name><affiliation><nlm:aff id="aff9">Steno Diabetes Center, Gentofte, Denmark;</nlm:aff></affiliation></author><author><name sortKey="Nierras, Concepcion" sort="Nierras, Concepcion" uniqKey="Nierras C" first="Concepcion" last="Nierras">Concepcion Nierras</name><affiliation><nlm:aff id="aff10">Juvenile Diabetes Research Foundation, New York, New York;</nlm:aff></affiliation></author><author><name sortKey="Pociot, Flemming" sort="Pociot, Flemming" uniqKey="Pociot F" first="Flemming" last="Pociot">Flemming Pociot</name><affiliation><nlm:aff id="aff9">Steno Diabetes Center, Gentofte, Denmark;</nlm:aff></affiliation></author><author><name sortKey="Todd, John A" sort="Todd, John A" uniqKey="Todd J" first="John A." last="Todd">John A. Todd</name><affiliation><nlm:aff id="aff11">Juvenile Diabetes Research Foundation/Wellcome Trust Diabetes and Inflammation Laboratory, Department of Medical Genetics, Cambridge Institute for Medical Research, University of Cambridge, Cambridge, U.K.</nlm:aff></affiliation></author><author><name sortKey="Rich, Stephen S" sort="Rich, Stephen S" uniqKey="Rich S" first="Stephen S." last="Rich">Stephen S. Rich</name><affiliation><nlm:aff id="aff2">Center for Public Health Genomics, University of Virginia, Charlottesville, Virginia;</nlm:aff></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmid">19136655</idno><idno type="pmc">2661598</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2661598</idno><idno type="RBID">PMC:2661598</idno><idno type="doi">10.2337/db08-1551</idno><date when="2009">2009</date><idno type="wicri:Area/Pmc/Corpus">002415</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">002415</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Genome-Wide Scan for Linkage to Type 1 Diabetes in 2,496 Multiplex Families From the Type 1 Diabetes Genetics Consortium</title><author><name sortKey="Concannon, Patrick" sort="Concannon, Patrick" uniqKey="Concannon P" first="Patrick" last="Concannon">Patrick Concannon</name><affiliation><nlm:aff id="aff1">Department of Biochemistry and Molecular Genetics, University of Virginia, Charlottesville, Virginia;</nlm:aff></affiliation><affiliation><nlm:aff id="aff2">Center for Public Health Genomics, University of Virginia, Charlottesville, Virginia;</nlm:aff></affiliation></author><author><name sortKey="Chen, Wei Min" sort="Chen, Wei Min" uniqKey="Chen W" first="Wei-Min" last="Chen">Wei-Min Chen</name><affiliation><nlm:aff id="aff2">Center for Public Health Genomics, University of Virginia, Charlottesville, Virginia;</nlm:aff></affiliation><affiliation><nlm:aff id="aff3">Department of Public Health Sciences, Division of Biostatistics and Epidemiology, University of Virginia, Charlottesville, Virginia;</nlm:aff></affiliation></author><author><name sortKey="Julier, Cecile" sort="Julier, Cecile" uniqKey="Julier C" first="Cécile" last="Julier">Cécile Julier</name><affiliation><nlm:aff id="aff4">INSERM U730, Centre National de Génotypage, Evry, France;</nlm:aff></affiliation></author><author><name sortKey="Morahan, Grant" sort="Morahan, Grant" uniqKey="Morahan G" first="Grant" last="Morahan">Grant Morahan</name><affiliation><nlm:aff id="aff5">Centre for Diabetes Research, The Western Australian Institute for Medical Research and Centre for Medical Research, University of Western Australia, Perth, Australia;</nlm:aff></affiliation></author><author><name sortKey="Akolkar, Beena" sort="Akolkar, Beena" uniqKey="Akolkar B" first="Beena" last="Akolkar">Beena Akolkar</name><affiliation><nlm:aff id="aff6">Division of Diabetes, Endocrinology, and Metabolic Diseases, The National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland;</nlm:aff></affiliation></author><author><name sortKey="Erlich, Henry A" sort="Erlich, Henry A" uniqKey="Erlich H" first="Henry A." last="Erlich">Henry A. Erlich</name><affiliation><nlm:aff id="aff7">Roche Molecular Systems, Pleasanton, California;</nlm:aff></affiliation></author><author><name sortKey="Hilner, Joan E" sort="Hilner, Joan E" uniqKey="Hilner J" first="Joan E." last="Hilner">Joan E. Hilner</name><affiliation><nlm:aff id="aff8">Public Health Sciences, Wake Forest University School of Medicine, Winston-Salem, North Carolina;</nlm:aff></affiliation></author><author><name sortKey="Nerup, J Rn" sort="Nerup, J Rn" uniqKey="Nerup J" first="J Rn" last="Nerup">J Rn Nerup</name><affiliation><nlm:aff id="aff9">Steno Diabetes Center, Gentofte, Denmark;</nlm:aff></affiliation></author><author><name sortKey="Nierras, Concepcion" sort="Nierras, Concepcion" uniqKey="Nierras C" first="Concepcion" last="Nierras">Concepcion Nierras</name><affiliation><nlm:aff id="aff10">Juvenile Diabetes Research Foundation, New York, New York;</nlm:aff></affiliation></author><author><name sortKey="Pociot, Flemming" sort="Pociot, Flemming" uniqKey="Pociot F" first="Flemming" last="Pociot">Flemming Pociot</name><affiliation><nlm:aff id="aff9">Steno Diabetes Center, Gentofte, Denmark;</nlm:aff></affiliation></author><author><name sortKey="Todd, John A" sort="Todd, John A" uniqKey="Todd J" first="John A." last="Todd">John A. Todd</name><affiliation><nlm:aff id="aff11">Juvenile Diabetes Research Foundation/Wellcome Trust Diabetes and Inflammation Laboratory, Department of Medical Genetics, Cambridge Institute for Medical Research, University of Cambridge, Cambridge, U.K.</nlm:aff></affiliation></author><author><name sortKey="Rich, Stephen S" sort="Rich, Stephen S" uniqKey="Rich S" first="Stephen S." last="Rich">Stephen S. Rich</name><affiliation><nlm:aff id="aff2">Center for Public Health Genomics, University of Virginia, Charlottesville, Virginia;</nlm:aff></affiliation></author></analytic><series><title level="j">Diabetes</title><idno type="ISSN">0012-1797</idno><idno type="eISSN">1939-327X</idno><imprint><date when="2009">2009</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><sec><title>OBJECTIVE</title><p>Type 1 diabetes arises from the actions of multiple genetic and environmental risk factors. Considerable success at identifying common genetic variants that contribute to type 1 diabetes risk has come from genetic association (primarily case-control) studies. However, such studies have limited power to detect genes containing multiple rare variants that contribute significantly to disease risk.</p></sec><sec><title>RESEARCH DESIGN AND METHODS</title><p>The Type 1 Diabetes Genetics Consortium (T1DGC) has assembled a collection of 2,496 multiplex type 1 diabetic families from nine geographical regions containing 2,658 affected sib-pairs (ASPs). We describe the results of a genome-wide scan for linkage to type 1 diabetes in the T1DGC family collection.</p></sec><sec><title>RESULTS</title><p>Significant evidence of linkage to type 1 diabetes was confirmed at the HLA region on chromosome 6p21.3 (logarithm of odds [LOD] = 213.2). There was further evidence of linkage to type 1 diabetes on 6q that could not be accounted for by the major linkage signal at the HLA class II loci on chromosome 6p21. Suggestive evidence of linkage (LOD ≥2.2) was observed near <italic>CTLA4</italic> on chromosome 2q32.3 (LOD = 3.28) and near <italic>INS</italic> (LOD = 3.16) on chromosome 11p15.5. Some evidence for linkage was also detected at two regions on chromosome 19 (LOD = 2.84 and 2.54).</p></sec><sec><title>CONCLUSIONS</title><p>Five non–HLA chromosome regions showed some evidence of linkage to type 1 diabetes. A number of previously proposed type 1 diabetes susceptibility loci, based on smaller ASP numbers, showed limited or no evidence of linkage to disease. Low-frequency susceptibility variants or clusters of loci with common alleles could contribute to the linkage signals observed.</p></sec></div></front><back><div1 type="bibliography"><listBibl><biblStruct><analytic><author><name sortKey="Davies, Jl" uniqKey="Davies J">JL Davies</name></author><author><name sortKey="Kawaguchi, Y" uniqKey="Kawaguchi Y">Y Kawaguchi</name></author><author><name sortKey="Bennett, St" uniqKey="Bennett S">ST Bennett</name></author><author><name sortKey="Copeman, Jb" uniqKey="Copeman J">JB Copeman</name></author><author><name sortKey="Cordell, Hj" uniqKey="Cordell H">HJ Cordell</name></author><author><name sortKey="Pritchard, Le" uniqKey="Pritchard L">LE Pritchard</name></author><author><name sortKey="Reed, Pw" uniqKey="Reed P">PW Reed</name></author><author><name sortKey="Gough, Sc" uniqKey="Gough S">SC Gough</name></author><author><name sortKey="Jenkins, Sc" uniqKey="Jenkins S">SC Jenkins</name></author><author><name sortKey="Palmer, Sm" uniqKey="Palmer 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<front><journal-meta><journal-id journal-id-type="nlm-ta">Diabetes</journal-id><journal-id journal-id-type="hwp">diabetes</journal-id><journal-id journal-id-type="pmc">diabetes</journal-id><journal-id journal-id-type="publisher-id">Diabetes</journal-id><journal-title-group><journal-title>Diabetes</journal-title></journal-title-group><issn pub-type="ppub">0012-1797</issn><issn pub-type="epub">1939-327X</issn><publisher><publisher-name>American Diabetes Association</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="pmid">19136655</article-id><article-id pub-id-type="pmc">2661598</article-id><article-id pub-id-type="publisher-id">1551</article-id><article-id pub-id-type="doi">10.2337/db08-1551</article-id><article-categories><subj-group subj-group-type="heading"><subject>Original Article</subject><subj-group><subject>Genetics</subject></subj-group></subj-group></article-categories><title-group><article-title>Genome-Wide Scan for Linkage to Type 1 Diabetes in 2,496 Multiplex Families From the Type 1 Diabetes Genetics Consortium</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Concannon</surname><given-names>Patrick</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="aff" rid="aff2"><sup>2</sup></xref><xref ref-type="corresp" rid="cor1"></xref></contrib><contrib contrib-type="author"><name><surname>Chen</surname><given-names>Wei-Min</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib><contrib contrib-type="author"><name><surname>Julier</surname><given-names>Cécile</given-names></name><xref ref-type="aff" rid="aff4"><sup>4</sup></xref></contrib><contrib contrib-type="author"><name><surname>Morahan</surname><given-names>Grant</given-names></name><xref ref-type="aff" rid="aff5"><sup>5</sup></xref></contrib><contrib contrib-type="author"><name><surname>Akolkar</surname><given-names>Beena</given-names></name><xref ref-type="aff" rid="aff6"><sup>6</sup></xref></contrib><contrib contrib-type="author"><name><surname>Erlich</surname><given-names>Henry A.</given-names></name><xref ref-type="aff" rid="aff7"><sup>7</sup></xref></contrib><contrib contrib-type="author"><name><surname>Hilner</surname><given-names>Joan E.</given-names></name><xref ref-type="aff" rid="aff8"><sup>8</sup></xref></contrib><contrib contrib-type="author"><name><surname>Nerup</surname><given-names>Jørn</given-names></name><xref ref-type="aff" rid="aff9"><sup>9</sup></xref></contrib><contrib contrib-type="author"><name><surname>Nierras</surname><given-names>Concepcion</given-names></name><xref ref-type="aff" rid="aff10"><sup>10</sup></xref></contrib><contrib contrib-type="author"><name><surname>Pociot</surname><given-names>Flemming</given-names></name><xref ref-type="aff" rid="aff9"><sup>9</sup></xref></contrib><contrib contrib-type="author"><name><surname>Todd</surname><given-names>John A.</given-names></name><xref ref-type="aff" rid="aff11"><sup>11</sup></xref></contrib><contrib contrib-type="author"><name><surname>Rich</surname><given-names>Stephen S.</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author"><collab>the Type 1 Diabetes Genetics Consortium</collab></contrib><aff id="aff1"><sup>1</sup>Department of Biochemistry and Molecular Genetics, University of Virginia, Charlottesville, Virginia;</aff><aff id="aff2"><sup>2</sup>Center for Public Health Genomics, University of Virginia, Charlottesville, Virginia;</aff><aff id="aff3"><sup>3</sup>Department of Public Health Sciences, Division of Biostatistics and Epidemiology, University of Virginia, Charlottesville, Virginia;</aff><aff id="aff4"><sup>4</sup>INSERM U730, Centre National de Génotypage, Evry, France;</aff><aff id="aff5"><sup>5</sup>Centre for Diabetes Research, The Western Australian Institute for Medical Research and Centre for Medical Research, University of Western Australia, Perth, Australia;</aff><aff id="aff6"><sup>6</sup>Division of Diabetes, Endocrinology, and Metabolic Diseases, The National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland;</aff><aff id="aff7"><sup>7</sup>Roche Molecular Systems, Pleasanton, California;</aff><aff id="aff8"><sup>8</sup>Public Health Sciences, Wake Forest University School of Medicine, Winston-Salem, North Carolina;</aff><aff id="aff9"><sup>9</sup>Steno Diabetes Center, Gentofte, Denmark;</aff><aff id="aff10"><sup>10</sup>Juvenile Diabetes Research Foundation, New York, New York;</aff><aff id="aff11"><sup>11</sup>Juvenile Diabetes Research Foundation/Wellcome Trust Diabetes and Inflammation Laboratory, Department of Medical Genetics, Cambridge Institute for Medical Research, University of Cambridge, Cambridge, U.K.</aff></contrib-group><author-notes><corresp id="cor1">Corresponding author: Patrick Concannon, <email>patcon@virginia.edu</email>.</corresp></author-notes><pub-date pub-type="ppub"><month>4</month><year>2009</year></pub-date><pub-date pub-type="epub"><day>9</day><month>1</month><year>2009</year></pub-date><volume>58</volume><issue>4</issue><fpage>1018</fpage><lpage>1022</lpage><history><date date-type="received"><day>6</day><month>11</month><year>2008</year></date><date date-type="accepted"><day>5</day><month>1</month><year>2009</year></date></history><permissions><copyright-statement>© 2009 by the American Diabetes Association.</copyright-statement><license license-type="creative-commons"><license-p>Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See <ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/licenses/by-nc-nd/3.0/">http://creativecommons.org/licenses/by-nc-nd/3.0/</ext-link> for details.</license-p></license></permissions><self-uri xlink:title="pdf" xlink:type="simple" xlink:href="zdb00409001018.pdf"></self-uri><abstract><sec><title>OBJECTIVE</title><p>Type 1 diabetes arises from the actions of multiple genetic and environmental risk factors. Considerable success at identifying common genetic variants that contribute to type 1 diabetes risk has come from genetic association (primarily case-control) studies. However, such studies have limited power to detect genes containing multiple rare variants that contribute significantly to disease risk.</p></sec><sec><title>RESEARCH DESIGN AND METHODS</title><p>The Type 1 Diabetes Genetics Consortium (T1DGC) has assembled a collection of 2,496 multiplex type 1 diabetic families from nine geographical regions containing 2,658 affected sib-pairs (ASPs). We describe the results of a genome-wide scan for linkage to type 1 diabetes in the T1DGC family collection.</p></sec><sec><title>RESULTS</title><p>Significant evidence of linkage to type 1 diabetes was confirmed at the HLA region on chromosome 6p21.3 (logarithm of odds [LOD] = 213.2). There was further evidence of linkage to type 1 diabetes on 6q that could not be accounted for by the major linkage signal at the HLA class II loci on chromosome 6p21. Suggestive evidence of linkage (LOD ≥2.2) was observed near <italic>CTLA4</italic> on chromosome 2q32.3 (LOD = 3.28) and near <italic>INS</italic> (LOD = 3.16) on chromosome 11p15.5. Some evidence for linkage was also detected at two regions on chromosome 19 (LOD = 2.84 and 2.54).</p></sec><sec><title>CONCLUSIONS</title><p>Five non–HLA chromosome regions showed some evidence of linkage to type 1 diabetes. A number of previously proposed type 1 diabetes susceptibility loci, based on smaller ASP numbers, showed limited or no evidence of linkage to disease. Low-frequency susceptibility variants or clusters of loci with common alleles could contribute to the linkage signals observed.</p></sec></abstract><funding-group><award-group><funding-source id="CS100">National Institutes of Health</funding-source><award-id rid="CS100">N01-HG-65403</award-id></award-group></funding-group></article-meta></front><body><p>Type 1 diabetes develops when the insulin-secreting β-cells in the pancreas are depleted by an autoimmune process of unknown origin. Diagnosis occurs when sufficient β-cell mass is lost that blood glucose levels cannot be maintained in the physiologic range. Although insulin treatment for type 1 diabetes is life saving, development of effective preventive therapies could be enhanced by improved prediction and a better understanding of the underlying disease mechanism, particularly events occurring during the extended preclinical period. Such considerations have motivated studies directed toward identifying the genetic risk factors that contribute to the disorder that might provide novel insights into disease etiology and targets for preventive therapy.</p><p>A number of genome-wide scans for linkage to type 1 diabetes have been reported (<xref ref-type="bibr" rid="B1">1</xref><xref ref-type="bibr" rid="B2"></xref><xref ref-type="bibr" rid="B3"></xref><xref ref-type="bibr" rid="B4"></xref><xref ref-type="bibr" rid="B5"></xref><xref ref-type="bibr" rid="B6"></xref>–<xref ref-type="bibr" rid="B7">7</xref>). All such studies consistently find evidence of linkage of type 1 diabetes to the HLA region on chromosome 6p21. An additional 15–20 regions with evidence of linkage to type 1 diabetes have been reported, but many of these regions have not been reproduced in independent studies. Several attempts have been made to address this problem through merging of datasets from different smaller studies (<xref ref-type="bibr" rid="B5">5</xref>,<xref ref-type="bibr" rid="B7">7</xref>), but differences in marker sets and allele coding have limited the power of these efforts.</p><p>To address issues of sample size and consistency and to clarify the evidence for linkage to type 1 diabetes, the Type 1 Diabetes Genetics Consortium (T1DGC) has conducted the largest affected sib-pair (ASP) linkage study in type 1 diabetes to date. This study includes many (<italic>n</italic> = 1,189) of the type 1 diabetes families used in previous smaller linkage studies, but the majority of families (<italic>n</italic> = 1,307) are newly recruited. More importantly, all samples, both retrospective and newly recruited, were independently genotyped expressly for this study at a single laboratory using a single platform and a common marker set. Analyses of these data provided evidence for linkage to type 1 diabetes in six regions on four different chromosomes.</p><sec><title>RESEARCH DESIGN AND METHODS</title><p>The families included in the analyses were ascertained from nine different sources: the four T1DGC regional networks of Asia-Pacific (<italic>n</italic> = 228), Europe (<italic>n</italic> = 585), North America (<italic>n</italic> = 370), and the U.K. (<italic>n</italic> = 124); the Diabetes UK Warren 1 Repository (<italic>n</italic> = 429); the Human Biological Data Interchange repository (<italic>n</italic> = 424); the Joslin Diabetes Center (<italic>n</italic> = 112); the Steno Diabetes Center (<italic>n</italic> = 146); and Sardinia (<italic>n</italic> = 78). To be included in the study, a family had to have at least one ASP available for sampling; availability of one or both biological parents was preferred but not required. An individual was designated as affected if he or she had documented type 1 diabetes with onset at <35 years of age, had used insulin within 6 months of diagnosis, and had no concomitant disease or disorder associated with diabetes. A total of 2,496 families were genotyped. Most families, 2,287 (91.6%), had exactly two affected full siblings, 101 (4.0%) had three, and 7 (0.3%) had four or more. Among 2,657 ASPs in total, both parents were available for 69.6% of the ASPs, 18.9% had only a single parent available, and 11.6% had neither parent available. A few extended pedigrees also provided 13 affected half-sib pairs and 22 affected-affected avuncular pairs.</p><sec><title>Genotyping.</title><p>Genotyping was carried out at the Center for Inherited Disease Research (CIDR) using the Illumina Human Linkage-12 Genotyping Beadchip, which contains 6,090 single nucleotide polymorphisms with an average genome-wide spacing of 0.58 cM.</p></sec><sec><title>Statistical analysis.</title><p>Before statistical genetic analyses, genotype data were evaluated for Mendelian errors using PedCheck (<xref ref-type="bibr" rid="B8">8</xref>). PREST (<xref ref-type="bibr" rid="B9">9</xref>) was used to estimate the likelihood of each specified relationship in pedigrees given the genotyping information. Based on these analyses, 43 families were removed from further analysis due to the presence of a duplicate family, a duplicate sample within the family, nonresolvable family errors, or missing genotype information. Merlin (<xref ref-type="bibr" rid="B10">10</xref>) was used to identify and resolve inconsistencies within families. Finally, 199 affected individuals who were not genotyped were removed from the analysis. The Kong and Cox linear nonparametric linkage (NPL) model (<xref ref-type="bibr" rid="B11">11</xref>) implemented in Merlin was used for the NPL linkage analysis. Marker-marker linkage disequilibrium was modeled in the linkage analysis using the maximum-likelihood clustered marker approach implemented in Merlin with a cutoff of <italic>r</italic><sup>2</sup> > 0.5.</p></sec></sec><sec sec-type="results"><title>RESULTS</title><p><xref ref-type="fig" rid="F1">Figure 1</xref> shows the results of the genome-wide analysis for linkage to type 1 diabetes in the entire T1DGC family collection. The average information content across all chromosomes was 0.924 and ranged from 0.904 on chromosome 20 to 0.939 on chromosomes six and X. <xref ref-type="table" rid="T1">Table 1</xref> lists the regions where evidence for linkage exceeded the threshold for suggestive linkage (logarithm of odds [LOD] ≥2.2) in an ASP linkage study. The HLA region on chromosome 6p21.3 was the only region to display significant evidence of linkage to type 1 diabetes (LOD = 213.2). Four additional regions provided suggestive evidence of linkage. These included a region on chromosome 2q (LOD = 3.28), where there have been multiple past reports of linkage to type 1 diabetes, and the region surrounding the insulin gene at 11p15.5 (LOD = 3.16) that has been previously implicated in type 1 diabetes susceptibility by both linkage and association studies. The remaining two regions were on chromosome 19 (LOD = 2.84 and 2.54) and are separated from each other by 48.5 cM; evidence of linkage to chromosome 19 has been reported before but not to any level of confidence that justified specific attention. Other previously reported type 1 diabetes loci, which quite often were given type 1 diabetes designations, were not confirmed in the current study (<xref ref-type="table" rid="T2">Table 2</xref>).</p><fig id="F1" position="float"><label>FIG. 1.</label><caption><p>Genome-wide evidence for linkage to type 1 diabetes. Evidence for linkage was evaluated using Merlin, and LOD scores were calculated using the Kong and Cox linear NPL model (<xref ref-type="bibr" rid="B10">10</xref>,<xref ref-type="bibr" rid="B11">11</xref>). LOD scores are plotted on the vertical axis versus chromosomal position on the horizontal axis. LOD scores at region 15.5–110.5 cM on chromosome 6 are larger than four and not shown. The dotted horizontal line indicates a LOD of 2.2. The dashed line indicates a LOD of 3.6.</p></caption><graphic xlink:href="zdb0040956880001"></graphic></fig><table-wrap id="T1" position="float"><label>TABLE 1</label><caption><p>Regions with suggestive or significant evidence of linkage to type 1 diabetes</p></caption><table frame="hsides" rules="groups"><thead valign="bottom"><tr><th align="left" rowspan="1" colspan="1">Chromosome</th><th align="center" rowspan="1" colspan="1">Position (cM)</th><th align="center" rowspan="1" colspan="1">LOD</th><th align="center" rowspan="1" colspan="1"><italic>P</italic></th><th align="center" rowspan="1" colspan="1">LOD-1 support interval</th><th align="center" rowspan="1" colspan="1">Flanking markers<xref ref-type="table-fn" rid="TF1-1">*</xref></th></tr></thead><tbody valign="top"><tr><td align="left" rowspan="1" colspan="1">2</td><td align="char" char="." rowspan="1" colspan="1">194.25</td><td align="char" char="." rowspan="1" colspan="1">3.28</td><td align="char" char="×" rowspan="1" colspan="1">5.0 × 10<sup>−5</sup></td><td align="char" char="–" rowspan="1" colspan="1">191.3–197.8</td><td align="left" rowspan="1" colspan="1"><italic>rs1882395</italic>/<italic>rs1369842</italic></td></tr><tr><td align="left" rowspan="1" colspan="1">6</td><td align="char" char="." rowspan="1" colspan="1">52.0</td><td align="char" char="." rowspan="1" colspan="1">213.2</td><td align="char" char="×" rowspan="1" colspan="1">8.0 × 10<sup>−216</sup></td><td align="char" char="–" rowspan="1" colspan="1">51.0–52.5</td><td align="left" rowspan="1" colspan="1"><italic>rs11908</italic>/<italic>rs412735</italic></td></tr><tr><td align="left" rowspan="1" colspan="1">11</td><td align="char" char="." rowspan="1" colspan="1">2.5</td><td align="char" char="." rowspan="1" colspan="1">3.16</td><td align="char" char="×" rowspan="1" colspan="1">7.0 × 10<sup>−5</sup></td><td align="char" char="–" rowspan="1" colspan="1">0–8.5</td><td align="left" rowspan="1" colspan="1"><italic>rs741737</italic>/<italic>rs1609812</italic></td></tr><tr><td align="left" rowspan="1" colspan="1">19</td><td align="char" char="." rowspan="1" colspan="1">9.5</td><td align="char" char="." rowspan="1" colspan="1">2.84</td><td align="char" char="." rowspan="1" colspan="1">0.00015</td><td align="char" char="–" rowspan="1" colspan="1">7.5–26</td><td align="left" rowspan="1" colspan="1"><italic>rs887270</italic>/<italic>rs1044250</italic></td></tr><tr><td align="left" rowspan="1" colspan="1">19</td><td align="char" char="." rowspan="1" colspan="1">58.0</td><td align="char" char="." rowspan="1" colspan="1">2.54</td><td align="char" char="." rowspan="1" colspan="1">0.0003</td><td align="char" char="–" rowspan="1" colspan="1">52–63</td><td align="left" rowspan="1" colspan="1"><italic>rs1019937</italic>/<italic>rs1878926</italic></td></tr></tbody></table><table-wrap-foot><fn id="TF1-1"><p>*Genotyped markers bounding the LOD-1 support interval.</p></fn></table-wrap-foot></table-wrap><table-wrap id="T2" position="float"><label>TABLE 2</label><caption><p>Evidence for linkage in regions previously reported to harbor <italic>IDDM</italic> loci</p></caption><table frame="hsides" rules="groups"><thead valign="bottom"><tr><th align="left" rowspan="1" colspan="1">Locus</th><th align="center" rowspan="1" colspan="1">Chromosome</th><th align="center" rowspan="1" colspan="1">Defined by marker(s)</th><th align="center" rowspan="1" colspan="1">Marker tested</th><th align="center" rowspan="1" colspan="1">LOD</th><th align="center" rowspan="1" colspan="1"><italic>P</italic></th></tr></thead><tbody valign="top"><tr><td align="left" rowspan="1" colspan="1"><italic>IDDM1</italic></td><td align="left" rowspan="1" colspan="1">6p21.3</td><td align="left" rowspan="1" colspan="1"><italic>HLA-DQ</italic>β<italic>1</italic></td><td align="left" rowspan="1" colspan="1"><italic>rs1019937</italic></td><td align="char" char="." rowspan="1" colspan="1">213.2</td><td align="char" char="×" rowspan="1" colspan="1">8.0 × 10<sup>−216</sup></td></tr><tr><td align="left" rowspan="1" colspan="1"><italic>IDDM2</italic></td><td align="left" rowspan="1" colspan="1">11p15.5</td><td align="left" rowspan="1" colspan="1"><italic>INS-VNTR</italic></td><td align="left" rowspan="1" colspan="1"><italic>rs1004446</italic></td><td align="char" char="." rowspan="1" colspan="1">3.09</td><td align="char" char="." rowspan="1" colspan="1">0.00008</td></tr><tr><td align="left" rowspan="1" colspan="1"><italic>IDDM3</italic></td><td align="left" rowspan="1" colspan="1">15q26</td><td align="left" rowspan="1" colspan="1"><italic>D15S107</italic></td><td align="left" rowspan="1" colspan="1"><italic>rs906310</italic></td><td align="char" char="." rowspan="1" colspan="1">0.00</td><td align="char" char="." rowspan="1" colspan="1">0.6</td></tr><tr><td align="left" rowspan="1" colspan="1"><italic>IDDM4</italic></td><td align="left" rowspan="1" colspan="1">11q13</td><td align="left" rowspan="1" colspan="1"><italic>D11S1917</italic></td><td align="left" rowspan="1" colspan="1"><italic>rs923346</italic></td><td align="char" char="." rowspan="1" colspan="1">0.87</td><td align="char" char="." rowspan="1" colspan="1">0.02</td></tr><tr><td align="left" rowspan="1" colspan="1"><italic>IDDM5</italic></td><td align="left" rowspan="1" colspan="1">6q25</td><td align="left" rowspan="1" colspan="1"><italic>ESR</italic></td><td align="left" rowspan="1" colspan="1"><italic>rs11902</italic></td><td align="char" char="." rowspan="1" colspan="1">0.00</td><td align="char" char="." rowspan="1" colspan="1">0.5</td></tr><tr><td align="left" rowspan="1" colspan="1"><italic>IDDM6</italic></td><td align="left" rowspan="1" colspan="1">18q</td><td align="left" rowspan="1" colspan="1"><italic>D18S64</italic></td><td align="left" rowspan="1" colspan="1"><italic>rs1943418</italic></td><td align="char" char="." rowspan="1" colspan="1">0.68</td><td align="char" char="." rowspan="1" colspan="1">0.04</td></tr><tr><td align="left" rowspan="1" colspan="1"><italic>IDDM7</italic></td><td align="left" rowspan="1" colspan="1">2q31</td><td align="left" rowspan="1" colspan="1"><italic>D2S152</italic></td><td align="left" rowspan="1" colspan="1"><italic>rs696092</italic></td><td align="char" char="." rowspan="1" colspan="1">1.91</td><td align="char" char="." rowspan="1" colspan="1">0.002</td></tr><tr><td align="left" rowspan="1" colspan="1"><italic>IDDM8</italic></td><td align="left" rowspan="1" colspan="1">6q27</td><td align="left" rowspan="1" colspan="1"><italic>D6S264</italic></td><td align="left" rowspan="1" colspan="1"><italic>rs6910121</italic></td><td align="char" char="." rowspan="1" colspan="1">0.45</td><td align="char" char="." rowspan="1" colspan="1">0.07</td></tr><tr><td align="left" rowspan="1" colspan="1"><italic>IDDM9</italic></td><td align="left" rowspan="1" colspan="1">3q21-25</td><td align="left" rowspan="1" colspan="1"><italic>D3S1303</italic></td><td align="left" rowspan="1" colspan="1"><italic>rs1983380</italic></td><td align="char" char="." rowspan="1" colspan="1">0.40</td><td align="char" char="." rowspan="1" colspan="1">0.09</td></tr><tr><td align="left" rowspan="1" colspan="1"><italic>IDDM10</italic></td><td align="left" rowspan="1" colspan="1">10cen</td><td align="left" rowspan="1" colspan="1"><italic>D10S193</italic></td><td align="left" rowspan="1" colspan="1"><italic>rs959629</italic></td><td align="char" char="." rowspan="1" colspan="1">1.07</td><td align="char" char="." rowspan="1" colspan="1">0.013</td></tr><tr><td align="left" rowspan="1" colspan="1"><italic>IDDM11</italic></td><td align="left" rowspan="1" colspan="1">14q24.3</td><td align="left" rowspan="1" colspan="1"><italic>D14S67</italic></td><td align="left" rowspan="1" colspan="1"><italic>rs1012921</italic></td><td align="char" char="." rowspan="1" colspan="1">0.13</td><td align="char" char="." rowspan="1" colspan="1">0.2</td></tr><tr><td align="left" rowspan="1" colspan="1"><italic>IDDM12</italic></td><td align="left" rowspan="1" colspan="1">2q33</td><td align="left" rowspan="1" colspan="1"><italic>CTLA4</italic></td><td align="left" rowspan="1" colspan="1"><italic>rs1947983</italic></td><td align="char" char="." rowspan="1" colspan="1">1.05</td><td align="char" char="." rowspan="1" colspan="1">0.014</td></tr><tr><td align="left" rowspan="1" colspan="1"><italic>IDDM13</italic></td><td align="left" rowspan="1" colspan="1">2q34</td><td align="left" rowspan="1" colspan="1"><italic>IGFBP2</italic></td><td align="left" rowspan="1" colspan="1"><italic>rs1851328</italic></td><td align="char" char="." rowspan="1" colspan="1">0.63</td><td align="char" char="." rowspan="1" colspan="1">0.04</td></tr><tr><td align="left" rowspan="1" colspan="1"><italic>IDDM15</italic></td><td align="left" rowspan="1" colspan="1">6q</td><td align="left" rowspan="1" colspan="1"><italic>D6S283</italic></td><td align="left" rowspan="1" colspan="1"><italic>rs2207958</italic></td><td align="char" char="." rowspan="1" colspan="1">5.99<xref ref-type="table-fn" rid="TF2-1">*</xref></td><td align="char" char="×" rowspan="1" colspan="1">7.5 × 10<sup>−8</sup></td></tr><tr><td align="left" rowspan="1" colspan="1"><italic>IDDM16</italic></td><td align="left" rowspan="1" colspan="1">14q32.3</td><td align="left" rowspan="1" colspan="1"><italic>D14S293</italic></td><td align="left" rowspan="1" colspan="1"><italic>rs872945</italic></td><td align="char" char="." rowspan="1" colspan="1">0.05</td><td align="char" char="." rowspan="1" colspan="1">0.3</td></tr><tr><td align="left" rowspan="1" colspan="1"><italic>IDDM17</italic></td><td align="left" rowspan="1" colspan="1">10q25</td><td align="left" rowspan="1" colspan="1"><italic>D10S592</italic></td><td align="left" rowspan="1" colspan="1"><italic>rs151603</italic></td><td align="char" char="." rowspan="1" colspan="1">0.16</td><td align="char" char="." rowspan="1" colspan="1">0.2</td></tr><tr><td align="left" rowspan="1" colspan="1"><italic>IDDM18</italic></td><td align="left" rowspan="1" colspan="1">5q33-34</td><td align="left" rowspan="1" colspan="1"><italic>IL12B</italic></td><td align="left" rowspan="1" colspan="1"><italic>rs270664</italic></td><td align="char" char="." rowspan="1" colspan="1">0.01</td><td align="char" char="." rowspan="1" colspan="1">0.4</td></tr><tr><td rowspan="1" colspan="1"></td><td align="left" rowspan="1" colspan="1">1q42</td><td align="left" rowspan="1" colspan="1"><italic>D1S1617</italic></td><td align="left" rowspan="1" colspan="1"><italic>rs342817</italic></td><td align="char" char="." rowspan="1" colspan="1">0.00</td><td align="char" char="." rowspan="1" colspan="1">0.5</td></tr><tr><td rowspan="1" colspan="1"></td><td align="left" rowspan="1" colspan="1">16q22-24</td><td align="left" rowspan="1" colspan="1"><italic>D16S3098</italic></td><td align="left" rowspan="1" colspan="1"><italic>rs1037973</italic></td><td align="char" char="." rowspan="1" colspan="1">1.24</td><td align="char" char="." rowspan="1" colspan="1">0.008</td></tr></tbody></table><table-wrap-foot><fn id="TF2-1"><p>*Not corrected for allele sharing at <italic>IDDM1</italic>. Adjustment based upon the expected LOD at <italic>D6S283</italic> and the recombination fraction with HLA yields an adjusted LOD of 2.7.</p></fn></table-wrap-foot></table-wrap><p>When considering evidence for linkage to type 1 diabetes on chromosome 6 that might possibly be due to loci other than the classic HLA genes, it was necessary to take into account the significant allele sharing at HLA, where LOD scores >3.6 were detected over an interval of ∼100 cM surrounding the locus. We searched for evidence of additional type 1 diabetes risk loci by calculating expected LOD (ELOD) scores based upon allele sharing at HLA along the length of chromosome 6 (supplementary Fig. 1, available in an online appendix at <ext-link ext-link-type="uri" xlink:href="http://diabetes.diabetesjournals.org/cgi/content/full/db08-1551/DC1">http://diabetes.diabetesjournals.org/cgi/content/full/db08-1551/DC1</ext-link>). The observed LOD score exceeded the ELOD by 3.6 in three regions. One of these regions, from 81.5 to 101.5 cM (maximum LOD − ELOD = 10.8), overlapped with the location of the previously reported <italic>IDDM15</italic> locus (<xref ref-type="bibr" rid="B6">6</xref>,<xref ref-type="bibr" rid="B12">12</xref>).</p></sec><sec sec-type="discussion"><title>DISCUSSION</title><p>The T1DGC family collection includes the largest number of ASPs to be tested for linkage to type 1 diabetes in a genome-wide scan yet provides suggestive or significant evidence for only five loci linked to type 1 diabetes. In light of the numerous previous reports of loci linked to type 1 diabetes, we considered the relationship between the findings here and prior studies (<xref ref-type="table" rid="T2">Table 2</xref>).</p><p>The majority of studies, as in our current report, have observed significant evidence of linkage to type 1 diabetes at HLA, and there is well-confirmed evidence of disease association in the same region. Several additional loci on chromosome 6 (<italic>IDDM5</italic>, <italic>IDDM8</italic>, and <italic>IDDM15</italic>) have been proposed based on previous linkage studies (<xref ref-type="bibr" rid="B1">1</xref>,<xref ref-type="bibr" rid="B13">13</xref>,<xref ref-type="bibr" rid="B14">14</xref>). The current study provides little support for either <italic>IDDM5</italic> or <italic>IDDM8</italic> (<xref ref-type="table" rid="T2">Table 2</xref>). However, we did obtain a regional maximum LOD of 5.43, at 190.0 cM on chromosome 6q27, where <italic>IDDM8</italic> was previously localized (<xref ref-type="bibr" rid="B13">13</xref>) when linkage disequilibrium was not modeled in the analysis. This region is characterized by a relatively strong intermarker linkage disequilibrium, which might explain this and previous reports of linkage in this region.</p><p>An additional region on chromosome 6q provided evidence for linkage to type 1 diabetes after adjusting for the effect of allele sharing at HLA. Previous studies have tested for linkage at <italic>IDDM15</italic>, which is located in this region, by calculating the expected LOD score at <italic>IDDM15</italic> based upon the observed identical-by-descent (IBD) sharing at HLA and the recombination fraction between HLA and <italic>D6S283</italic> (<xref ref-type="bibr" rid="B7">7</xref>,<xref ref-type="bibr" rid="B12">12</xref>). The excess of the observed IBD sharing compared with that which was expected was then used as a measure of the independent contribution of <italic>IDDM15</italic>. Applying this approach to the current dataset identified a broad (20 cM) region where the adjusted LOD exceeds 3.6. Uncertainties remain as to the precise location of <italic>IDDM15</italic> because male and female recombination maps differ substantially in this region. Nevertheless, this region of increased LODs, after adjusting for the contribution of allele sharing at HLA, provides support for the existence of an additional linkage to type 1 diabetes in this region.</p><p>Chromosome 2q contains two confirmed type 1 diabetes risk loci near the <italic>IFIH1</italic> and <italic>CTLA4</italic> genes identified by association and three proposed loci (<italic>IDDM7</italic>, <italic>IDDM12</italic>, and <italic>IDDM13</italic>) for which suggestive evidence of linkage has been observed in some, but not all, studies (<xref ref-type="bibr" rid="B15">15</xref><xref ref-type="bibr" rid="B16"></xref>–<xref ref-type="bibr" rid="B17">17</xref>). In the current report, there was no support for multiple distinct loci; suggestive evidence of linkage was observed in the 2q32.3 region, approximately midway between the previously proposed locations of <italic>IDDM7</italic> and <italic>IDDM12</italic>. The <italic>INS</italic> locus at 11p15.5 is also well established as a risk locus for type 1 diabetes (<xref ref-type="bibr" rid="B18">18</xref>). Previous studies have provided significant evidence for both association and linkage to this site. The current study also finds suggestive evidence of linkage in this region.</p><p>Two regions on chromosome 19 displayed suggestive evidence of linkage to type 1 diabetes, which, given our sample sizes and marker map, is the most interesting data yet for this chromosome. So far, no associations with genome-wide significance have been reported in these regions.</p><p>Recently, genome-wide association (GWA) studies have identified at least 18 genomic regions with significant evidence of association to type 1 diabetes, but the majority of these loci, although common in the population, have relatively modest individual effects on risk (e.g., odds ratios [ORs] of 1.1–1.3) (<xref ref-type="bibr" rid="B19">19</xref><xref ref-type="bibr" rid="B20"></xref><xref ref-type="bibr" rid="B21"></xref>–<xref ref-type="bibr" rid="B22">22</xref>). Linkage studies are not optimal for detecting such loci where the risk alleles are common and have small individual effect sizes. Thus, it is not surprising that none of these newly identified loci from GWA studies fall within regions of even suggestive linkage in the current study. Several of our linkage peaks do include loci previously detected by association, but these tend to have large effects on risk such as HLA (OR 11.4) (<xref ref-type="bibr" rid="B23">23</xref>) or <italic>INS</italic> (2.38) (<xref ref-type="bibr" rid="B18">18</xref>).</p><p>The large sample size studied here, 2,658 ASPs from 2,496 families, provided us with unprecedented power to detect linkage to type 1 diabetes across the genome. While we detected one locus with significant evidence of linkage, and five more regions with suggestive evidence, our study provides little support for the majority of previously proposed type 1 diabetes loci. Our power to detect evidence of linkage to type 1 diabetes comes at a cost; the low frequency of families with multiple affected siblings required a world-wide recruitment effort. Therefore, we cannot exclude the possibility that loci with strong effects in particular populations might be obscured in the current analysis. For example, LOD = 3.21 was observed at 66.1 cM on chromosome 17 in the 370 T1DGC families recruited by the North American network, whereas no linkage was detected in the other eight populations (LOD scores ranging from −0.62 to 0.30).</p><p>In summary, the evidence for independent major gene effects in type 1 diabetes detectable by linkage (e.g., rare variants), which are shared across populations, appears to be limited to a few genes in the HLA complex: <italic>INS</italic>, <italic>CTLA4</italic>, <italic>IDDM15</italic>, and possibly two regions on chromosomes 19. The combination of these putative rare variant effects with common variants of smaller effect size, more readily detected by association-based approaches, accounts for the majority of risk for type 1 diabetes of which HLA class II alleles are by far the major contributor. Identification of candidate genes and variants in these and other regions will help to clarify the biochemical pathways and mechanisms that contribute to risk for this common autoimmune disease. The substantial collection of biospecimens and data assembled by the T1DGC, and available to diabetes researchers (<ext-link ext-link-type="uri" xlink:href="http://www.t1dgc.org">www.t1dgc.org</ext-link> and <ext-link ext-link-type="uri" xlink:href="http://www.t1dbase.org">www.t1dbase.org</ext-link>), should be an important resource for further characterizing those genomic regions identified by either linkage or association approaches as contributing to risk for type 1 diabetes.</p></sec><sec sec-type="supplementary-material"><title>Supplementary Material</title><supplementary-material id="PMC_1" content-type="local-data"><caption><title>Online-Only Appendix</title></caption><media mimetype="text" mime-subtype="html" xlink:href="supp_58_4_1018__index.html"></media><media xlink:role="associated-file" mimetype="application" mime-subtype="msword" xlink:href="supp_db08-1551_db08-15511.suppl.doc"></media></supplementary-material></sec></body><back><fn-group><fn fn-type="financial-disclosure"><p>The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked “advertisement” in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.</p></fn></fn-group><ack><title>Acknowledgments</title><p>This research utilizes resources provided by the Type 1 Diabetes Genetics Consortium, a collaborative clinical study sponsored by the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), National Institute of Allergy and Infectious Diseases (NIAID), National Human Genome Research Institute (NHGRI), National Institute of Child Health and Human Development (NICHD), and Juvenile Diabetes Research Foundation International (JDRF) and supported by U01 DK062418. Further support was provided by a grant from the NIDDK (DK46635) to P.C. and a joint JDRF and Wellcome Trust grant to the Diabetes and Inflammation Laboratory at Cambridge, which also received support from the National Institute for Health Research Cambridge Biomedical Research Centre. Genotyping was performed by the Center for Inherited Disease Research (CIDR). CIDR is fully funded through a federal contract from the National Institutes of Health to the Johns Hopkins University, contract no. 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