Population-based rare variant detection via pooled exome or custom hybridization capture with or without individual indexing
about
Rare variants in FBN1 and FBN2 are associated with severe adolescent idiopathic scoliosisMultiplexed direct genomic selection (MDiGS): a pooled BAC capture approach for highly accurate CNV and SNP/INDEL detection.Excess congenital non-synonymous variation in leukemia-associated genes in MLL- infant leukemia: a Children's Oncology Group report.Accuracy of allele frequency estimation using pooled RNA-Seq.Accurate detection of subclonal single nucleotide variants in whole genome amplified and pooled cancer samples using HaloPlex target enrichment.Efficient Genome-Wide Detection and Cataloging of EMS-Induced Mutations Using Exome Capture and Next-Generation Sequencing.Genetic Analysis of Substrain Divergence in Non-Obese Diabetic (NOD) MiceCandidate gene resequencing to identify rare, pedigree-specific variants influencing healthy aging phenotypes in the long life family study.The minimal amount of starting DNA for Agilent's hybrid capture-based targeted massively parallel sequencingVarElect: the phenotype-based variation prioritizer of the GeneCards Suite.Targeted sequencing of both DNA strands barcoded and captured individually by RNA probes to identify genome-wide ultra-rare mutations.Targeted single molecule mutation detection with massively parallel sequencing.Exome sequencing in pooled DNA samples to identify maternal pre-eclampsia risk variants.Genetic variation in MKL2 and decreased downstream PCTAIRE1 expression in extreme, fatal primary human microcephaly.
P2860
Q28240167-1C6B0DB3-0E3E-4058-8AC9-44F4F0CBFB06Q33698461-92F543F7-DC81-4726-9DC1-7595D1D7D9DAQ33711624-909460A3-C0BA-492D-AB82-AB3FFAD83A23Q35015999-9A28DA3A-0658-450A-BB11-DF8077B7D4C0Q35061962-D244AC0B-F41A-4F68-BB08-D728E70A9C4AQ35147024-6214D260-6E3C-4152-B741-AEBE8AD38E80Q35589982-D6C688AD-E80C-4C54-A746-E02C83C6CD16Q35984424-14430312-D430-4FB0-807C-092157857D99Q36028346-0826CF7B-6B7B-4D00-B078-2AF4C873FBA1Q36064361-039867A3-3D07-4FB8-9136-C4A04FD76380Q36404734-AA32B3C8-D64A-4D0E-A12B-070ABF908329Q36588964-0A412F7F-90C1-46A3-B3DF-93AA6A1CD947Q37072661-6FAF5A4D-F0D0-488A-85D7-D4D58EE3937AQ37593826-4295AB86-3F07-4756-B340-F6FC467D62EA
P2860
Population-based rare variant detection via pooled exome or custom hybridization capture with or without individual indexing
description
2012 nî lūn-bûn
@nan
2012 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի դեկտեմբերին 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
Population-based rare variant ...... or without individual indexing
@ast
Population-based rare variant ...... or without individual indexing
@en
Population-based rare variant ...... or without individual indexing
@nl
type
label
Population-based rare variant ...... or without individual indexing
@ast
Population-based rare variant ...... or without individual indexing
@en
Population-based rare variant ...... or without individual indexing
@nl
prefLabel
Population-based rare variant ...... or without individual indexing
@ast
Population-based rare variant ...... or without individual indexing
@en
Population-based rare variant ...... or without individual indexing
@nl
P2093
P2860
P356
P1433
P1476
Population-based rare variant ...... or without individual indexing
@en
P2093
Andrew Hughes
Andrew L Young
Benjamin T Levinson
Enrique Ramos
Francesco L M Vallania
Katherine Thornton
Sara Chasnoff
P2860
P356
10.1186/1471-2164-13-683
P407
P577
2012-12-06T00:00:00Z