Detecting and estimating contamination of human DNA samples in sequencing and array-based genotype data.
about
Rare-variant association analysis: study designs and statistical testsExome sequencing and complex disease: practical aspects of rare variant association studiesGenome sequencing elucidates Sardinian genetic architecture and augments association analyses for lipid and blood inflammatory markersIron Age and Anglo-Saxon genomes from East England reveal British migration historyAMMECR1: a single point mutation causes developmental delay, midface hypoplasia and elliptocytosisThe genetic architecture of type 2 diabetesMultiple Hepatic Regulatory Variants at the GALNT2 GWAS Locus Associated with High-Density Lipoprotein CholesterolExome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction.Identification of Novel Variants in LTBP2 and PXDN Using Whole-Exome Sequencing in Developmental and Congenital GlaucomaIn search of rare variants: preliminary results from whole genome sequencing of 1,325 individuals with psychophysiological endophenotypes.SASI-Seq: sample assurance Spike-Ins, and highly differentiating 384 barcoding for Illumina sequencing.An efficient and scalable analysis framework for variant extraction and refinement from population-scale DNA sequence data.Correcting for Sample Contamination in Genotype Calling of DNA Sequence Data.Identification and Correction of Sample Mix-Ups in Expression Genetic Data: A Case StudyThe Genomic Scrapheap Challenge; Extracting Relevant Data from Unmapped Whole Genome Sequencing Reads, Including Strain Specific Genomic Segments, in Rats.From next-generation resequencing reads to a high-quality variant data set.Parasite infection of public databases: a data mining approach to identify apicomplexan contaminations in animal genome and transcriptome assemblies.Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity.Ancestry estimation and control of population stratification for sequence-based association studies.Health and population effects of rare gene knockouts in adult humans with related parentsTranscriptional diversity during lineage commitment of human blood progenitors.Common contaminants in next-generation sequencing that hinder discovery of low-abundance microbesHuman phenotype ontology annotation and cluster analysis to unravel genetic defects in 707 cases with unexplained bleeding and platelet disorders.Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways.Exome Sequencing in Classic Hairy Cell Leukaemia Reveals Widespread Variation in Acquired Somatic Mutations between Individual Tumours Apart from the Signature BRAF V(600)E Lesion.Peptidomic and transcriptomic profiling of four distinct spider venomsABCA7 rare variants and Alzheimer disease riskThe genetic regulatory signature of type 2 diabetes in human skeletal muscle.Identification of a rare coding variant in complement 3 associated with age-related macular degenerationIdentifying rare variants associated with complex traits via sequencing.Quality Control for the Illumina HumanExome BeadChip.Batch effects and the effective design of single-cell gene expression studies.The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.Genetic regulatory signatures underlying islet gene expression and type 2 diabetes.A SNP profiling panel for sample tracking in whole-exome sequencing studies.A novel post hoc method for detecting index switching finds no evidence for increased switching on the Illumina HiSeq X.Human pluripotent stem cells recurrently acquire and expand dominant negative P53 mutations.MBV: a method to solve sample mislabeling and detect technical bias in large combined genotype and sequencing assay datasets.17q21.31 duplication causes prominent tau-related dementia with increased MAPT expression.Mycoplasma contamination in the 1000 Genomes Project.
P2860
Q26852733-985502ED-B04A-48B3-9587-14AE0AB7DE7CQ27027055-957408AA-ADBD-446E-88E8-9043036C0333Q28267312-89BB6429-28C6-431C-87E1-6755B0897ADFQ28601637-65026439-6C1A-4743-A88B-255AF623C7E3Q28975784-DEBC6E08-778A-47DF-8ED6-14B56B7308F4Q29583824-7347105F-C91A-441D-B0E4-8F528388AFBBQ30277960-74F9988B-9A43-4B7D-8137-16B59CDF8BEFQ30301147-5871230C-3161-4F69-BB31-918A32536ACEQ30377934-A7BA4FA5-4232-4558-A330-3BB9224E7957Q30397608-6313CF0C-1B71-470C-8112-E52230DF6321Q30438936-C6A802C7-EC4A-4F17-947E-66E4724EF717Q30934831-5E86E12F-21BE-484B-AF82-BE9BCDF5413FQ30984579-B3D1D4B4-36AA-420D-8FBE-303E230B6EE5Q30988329-30492D7B-7739-403D-B547-5D2AE1F35777Q31120231-0EB08E11-1FAE-4155-B7C5-59A57B254A7FQ31137675-37DE889F-14B2-43DF-8ABC-AAE11DA7B19CQ31155417-5FE499EF-3265-48E0-A1F9-D0E06D7171C0Q33854345-2125E2E2-274D-4688-BE35-DBBB14819448Q33856061-66E2B4C4-47D8-43D1-AC40-1229B9C90495Q34046351-2916ED31-0ECB-4473-BE20-A364E67F0C8BQ34626417-9D47408E-3881-427C-96A2-C0D1D4A43981Q35170475-51DBC0D4-5ADB-46D0-B61B-2B636E6BA52EQ35577026-8E5CAB77-0CC8-482B-82EC-A0D99D020A69Q35624305-16D4144B-E3B1-4310-B296-1C26B7268BF4Q35922137-3D46C6DA-660C-47A4-B5B8-76B5ECB8F110Q36312190-A6BC1B7F-4F3E-499D-84A2-1FBA791101AAQ36982034-F9233B8C-B2B8-4D28-B89F-50DA159397AAQ37060991-D7D424C9-A55E-4E2E-8A53-370F314164F6Q37265929-3AAF7DD5-A0C7-49B7-8ADC-EE9895383EA4Q37316697-060A212A-C497-4CDF-8DC0-182DBABC1389Q37401251-29A96863-5D0F-4CE6-8D61-DCD0B58670C5Q37550421-858AFCF6-212B-46CE-9AD6-366DF6CA011DQ37634534-B40B48CC-D14B-4AAB-8083-0D25DA709382Q37682430-9E203048-9FD7-4EB7-81F2-600D678D75E5Q37690640-152DA1FF-0644-4B88-86F6-4990F67DB30DQ38620152-203BABC8-0329-4557-9A45-E64F2FA75B88Q38705984-E932C8A8-7E06-415D-8084-FCFDE7665EC5Q38967821-C8198E00-3C72-41C1-8EA4-4DEFFFC6E8ADQ39107119-0EBA9150-C64D-481C-BEB0-0207B05E81CFQ39646275-E05361B4-183C-47FF-A23C-510BEECF7FA6
P2860
Detecting and estimating contamination of human DNA samples in sequencing and array-based genotype data.
description
2012 nî lūn-bûn
@nan
2012 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
name
Detecting and estimating conta ...... and array-based genotype data.
@ast
Detecting and estimating conta ...... and array-based genotype data.
@en
Detecting and estimating conta ...... and array-based genotype data.
@en-gb
type
label
Detecting and estimating conta ...... and array-based genotype data.
@ast
Detecting and estimating conta ...... and array-based genotype data.
@en
Detecting and estimating conta ...... and array-based genotype data.
@en-gb
prefLabel
Detecting and estimating conta ...... and array-based genotype data.
@ast
Detecting and estimating conta ...... and array-based genotype data.
@en
Detecting and estimating conta ...... and array-based genotype data.
@en-gb
P2093
P2860
P50
P1476
Detecting and estimating conta ...... and array-based genotype data.
@en
P2093
Hyun Min Kang
Jane M Romm
Kimberly F Doheny
Kurt N Hetrick
Matthew Flickinger
P2860
P304
P356
10.1016/J.AJHG.2012.09.004
P407
P577
2012-10-25T00:00:00Z