Serveur d'exploration MERS - Curation (PubMed)

Index « MedMesh.i » - entrée « Genome, Human »
Attention, ce site est en cours de développement !
Attention, site généré par des moyens informatiques à partir de corpus bruts.
Les informations ne sont donc pas validées.
Genome, Helminth < Genome, Human < Genome, Insect  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 46.
[0-20] [0 - 20][0 - 46][20-40]
Ident.Authors (with country if any)Title
000531 (2019) Katarzyna Wreczycka [Allemagne] ; Vedran Franke [Allemagne] ; Bora Uyar [Allemagne] ; Ricardo Wurmus [Allemagne] ; Selman Bulut [Allemagne] ; Baris Tursun [Allemagne] ; Altuna Akalin [Allemagne]HOT or not: examining the basis of high-occupancy target regions.
000592 (2019) Weiling Li [États-Unis] ; Lin Lin [États-Unis] ; Raunaq Malhotra [États-Unis] ; Lei Yang [États-Unis] ; Raj Acharya [États-Unis] ; Mary Poss [États-Unis]A computational framework to assess genome-wide distribution of polymorphic human endogenous retrovirus-K In human populations.
000678 (2019) Wentian Li [États-Unis] ; Jerome Freudenberg [États-Unis] ; Jan Freudenberg [États-Unis]Alignment-free approaches for predicting novel Nuclear Mitochondrial Segments (NUMTs) in the human genome.
000863 (2018) Jonas Andreas Sibbesen [Danemark] ; Lasse Maretty [Danemark] ; Anders Krogh [Danemark]Accurate genotyping across variant classes and lengths using variant graphs.
000975 (2019) Yun Jia [République populaire de Chine] ; Hong Li [République populaire de Chine] ; Jingfeng Wang [République populaire de Chine] ; Hu Meng [République populaire de Chine] ; Zhenhua Yang [République populaire de Chine]Spectrum structures and biological functions of 8-mers in the human genome.
000A06 (2018) Meznah Almutairy [États-Unis] ; Eric Torng [États-Unis]Comparing fixed sampling with minimizer sampling when using k-mer indexes to find maximal exact matches.
000B26 (????) Tony Pan ; Patrick Flick ; Chirag Jain ; Yongchao Liu ; Srinivas AluruKmerind: A Flexible Parallel Library for K-mer Indexing of Biological Sequences on Distributed Memory Systems.
000B33 (2017) Yaron Orenstein [États-Unis] ; David Pellow [Israël] ; Guillaume Marçais [États-Unis] ; Ron Shamir [Israël] ; Carl Kingsford [États-Unis]Designing small universal k-mer hitting sets for improved analysis of high-throughput sequencing.
000B64 (2017) Guillaume Marçais [États-Unis] ; David Pellow [Israël] ; Daniel Bork [États-Unis] ; Yaron Orenstein [États-Unis] ; Ron Shamir [Israël] ; Carl Kingsford [États-Unis]Improving the performance of minimizers and winnowing schemes.
000C31 (2017) Meznah Almutairy [États-Unis] ; Eric Torng [États-Unis]The effects of sampling on the efficiency and accuracy of k-mer indexes: Theoretical and empirical comparisons using the human genome.
000C77 (2017) Fanny-Dhelia Pajuste [Estonie] ; Lauris Kaplinski [Estonie] ; M Rt Möls [Estonie] ; Tarmo Puurand [Estonie] ; Maarja Lepamets [Estonie] ; Maido Remm [Estonie]FastGT: an alignment-free method for calling common SNVs directly from raw sequencing reads.
000D01 (2017) Hamid Mohamadi [Canada] ; Hamza Khan [Canada] ; Inanc Birol [Canada]ntCard: a streaming algorithm for cardinality estimation in genomics data.
000D17 (2017) Abedalrhman Alkhateeb [Canada] ; Luis Rueda [Canada]Zseq: An Approach for Preprocessing Next-Generation Sequencing Data.
000E47 (2017) Dirk D. Dolle [Royaume-Uni] ; Zhicheng Liu [Royaume-Uni] ; Matthew Cotten [Royaume-Uni] ; Jared T. Simpson [Canada] ; Zamin Iqbal [Royaume-Uni] ; Richard Durbin [Royaume-Uni] ; Shane A. Mccarthy [Royaume-Uni] ; Thomas M. Keane [Royaume-Uni]Using reference-free compressed data structures to analyze sequencing reads from thousands of human genomes.
000F79 (2016) Ariya Shajii [États-Unis] ; Deniz Yorukoglu ; Yun William Yu [États-Unis] ; Bonnie Berger [États-Unis]Fast genotyping of known SNPs through approximate k-mer matching.
001195 (2016) Wenxuan Xu [République populaire de Chine] ; Li Zhang [République populaire de Chine] ; Yaping Lu [République populaire de Chine]SD-MSAEs: Promoter recognition in human genome based on deep feature extraction.
001432 (2016) Haoyang Zeng ; Tatsunori Hashimoto ; Daniel D. Kang ; David K. Gifford [États-Unis]GERV: a statistical method for generative evaluation of regulatory variants for transcription factor binding.
001805 (2014) Páll Melsted [Islande] ; Bjarni V. Halld Rsson [Islande]KmerStream: streaming algorithms for k-mer abundance estimation.
001824 (2014) Jiannan Guo [États-Unis] ; Tiandao Li ; Joshua Schipper ; Kyle A. Nilson ; Francis K. Fordjour ; Jeffrey J. Cooper ; Raluca Gordân ; David H. PriceSequence specificity incompletely defines the genome-wide occupancy of Myc.
001933 (2014) Lilian Janin [Royaume-Uni] ; Ole Schulz-Trieglaff [Royaume-Uni] ; Anthony J. Cox [Royaume-Uni]BEETL-fastq: a searchable compressed archive for DNA reads.
001963 (2014) Jia Wen [Hong Kong] ; Raymond H F. Chan [Hong Kong] ; Shek-Chung Yau [Hong Kong] ; Rong L. He [États-Unis] ; Stephen S T. Yau [République populaire de Chine]K-mer natural vector and its application to the phylogenetic analysis of genetic sequences.

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Sante/explor/MersV1/Data/PubMed/Curation
HfdIndexSelect -h $EXPLOR_AREA/Data/PubMed/Curation/MedMesh.i -k "Genome, Human" 
HfdIndexSelect -h $EXPLOR_AREA/Data/PubMed/Curation/MedMesh.i  \
                -Sk "Genome, Human" \
         | HfdSelect -Kh $EXPLOR_AREA/Data/PubMed/Curation/biblio.hfd 

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Sante
   |area=    MersV1
   |flux=    PubMed
   |étape=   Curation
   |type=    indexItem
   |index=    MedMesh.i
   |clé=    Genome, Human
}}

Wicri

This area was generated with Dilib version V0.6.33.
Data generation: Mon Apr 20 23:26:43 2020. Site generation: Sat Mar 27 09:06:09 2021