Variant identification in multi-sample pools by illumina genome analyzer sequencing
about
Germline mutations in NFKB2 implicate the noncanonical NF-κB pathway in the pathogenesis of common variable immunodeficiencyVarBin, a novel method for classifying true and false positive variants in NGS data.Determination of RET Sequence Variation in an MEN2 Unaffected Cohort Using Multiple-Sample Pooling and Next-Generation SequencingEmpirical validation of pooled whole genome population re-sequencing in Drosophila melanogasterGenetic Variants Associated with Port-Wine Stains.Validation of SNP allele frequencies determined by pooled next-generation sequencing in natural populations of a non-model plant species.Whole exome sequencing in neurogenetic odysseys: An effective, cost- and time-saving diagnostic approach.A new approach based on targeted pooled DNA sequencing identifies novel mutations in patients with Inherited Retinal Dystrophies
P2860
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P2860
Variant identification in multi-sample pools by illumina genome analyzer sequencing
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
2011年论文
@zh
2011年论文
@zh-cn
name
Variant identification in multi-sample pools by illumina genome analyzer sequencing
@en
Variant identification in multi-sample pools by illumina genome analyzer sequencing
@nl
type
label
Variant identification in multi-sample pools by illumina genome analyzer sequencing
@en
Variant identification in multi-sample pools by illumina genome analyzer sequencing
@nl
prefLabel
Variant identification in multi-sample pools by illumina genome analyzer sequencing
@en
Variant identification in multi-sample pools by illumina genome analyzer sequencing
@nl
P2093
P2860
P1476
Variant identification in multi-sample pools by illumina genome analyzer sequencing
@en
P2093
David C Pattison
Jack E Stephens
Jacob D Durtschi
Karl V Voelkerding
Rebecca L Margraf
Shale Dames
P2860
P577
2011-07-01T00:00:00Z