HLA typing from 1000 genomes whole genome and whole exome illumina data.
about
Overview of recurrent chromosomal losses in retinoblastoma detected by low coverage next generation sequencingThe impact of next-generation sequencing technologies on HLA researchThe relevance of HLA sequencing in population genetics studiesComparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association Study.OptiType: precision HLA typing from next-generation sequencing data.HLA-VBSeq: accurate HLA typing at full resolution from whole-genome sequencing data.Mapping Bias Overestimates Reference Allele Frequencies at the HLA Genes in the 1000 Genomes Project Phase I Data.Evaluation of computational programs to predict HLA genotypes from genomic sequencing data.Prediction and prioritization of neoantigens: integration of RNA sequencing data with whole-exome sequencing.HLAscan: genotyping of the HLA region using next-generation sequencing data.Inference of high resolution HLA types using genome-wide RNA or DNA sequencing readsHLA diversity in the 1000 genomes dataset.A Bead-based Normalization for Uniform Sequencing depth (BeNUS) protocol for multi-samples sequencing exemplified by HLA-B.Current and emerging Legionella diagnostics for laboratory and outbreak investigations.HLAreporter: a tool for HLA typing from next generation sequencing dataDevelopment and validation of a sample sparing strategy for HLA typing utilizing next generation sequencing.Granuloma genes in sarcoidosis: what is new?Association of HLA-DRB1 genetic variants with the persistence of atopic dermatitis.HLA-HD: An accurate HLA typing algorithm for next-generation sequencing data.Droplet Barcode Sequencing for targeted linked-read haplotyping of single DNA molecules.PGRNseq: a targeted capture sequencing panel for pharmacogenetic research and implementation.Considerations for rare variants in drug metabolism genes and the clinical implications.A genomic perspective on HLA evolution.Towards allele-level human leucocyte antigens genotyping - assessing two next-generation sequencing platforms: Ion Torrent Personal Genome Machine and Illumina MiSeq.Haplotyping the human leukocyte antigen system from single chromosomes.Development of a high-resolution NGS-based HLA-typing and analysis pipelineHLAProfiler utilizes k-mer profiles to improve HLA calling accuracy for rare and common alleles in RNA-seq data.Deciphering the fine nucleotide diversity of full HLA class I and class II genes in a well-documented population from sub-Saharan Africa.Accuracy of Programs for the Determination of Human Leukocyte Antigen Alleles from Next-Generation Sequencing Data.What has GWAS done for HLA and disease associations?Kourami: graph-guided assembly for novel human leukocyte antigen allele discovery.Multiplexed Nanopore Sequencing of HLA-B Locus in Māori and Pacific Island Samples.
P2860
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P2860
HLA typing from 1000 genomes whole genome and whole exome illumina data.
description
2013 nî lūn-bûn
@nan
2013 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
HLA typing from 1000 genomes whole genome and whole exome illumina data.
@ast
HLA typing from 1000 genomes whole genome and whole exome illumina data.
@en
type
label
HLA typing from 1000 genomes whole genome and whole exome illumina data.
@ast
HLA typing from 1000 genomes whole genome and whole exome illumina data.
@en
prefLabel
HLA typing from 1000 genomes whole genome and whole exome illumina data.
@ast
HLA typing from 1000 genomes whole genome and whole exome illumina data.
@en
P2093
P2860
P1433
P1476
HLA typing from 1000 genomes whole genome and whole exome illumina data.
@en
P2093
Attila Bérces
Endre Major
Krisztina Rigó
Szilveszter Juhos
P2860
P304
P356
10.1371/JOURNAL.PONE.0078410
P407
P577
2013-11-06T00:00:00Z