about
Frequent mutation of BAP1 in metastasizing uveal melanomasTargeted enrichment of genomic DNA regions for next-generation sequencingSequencing and analysis of Neanderthal genomic DNARare variants in FBN1 and FBN2 are associated with severe adolescent idiopathic scoliosisSolution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencingSomatic coding mutations in human induced pluripotent stem cellsHybrid selection of discrete genomic intervals on custom-designed microarrays for massively parallel sequencingSNPAAMapper: An efficient genome-wide SNP variant analysis pipeline for next-generation sequencing dataThird generation sequencing technologies applied to diagnostic microbiology: benefits and challenges in applications and data analysis.Preparing a re-sequencing DNA library of 2 cancer candidate genes using the ligation-by-amplification protocol by two PCR reactions.Filter-based hybridization capture of subgenomes enables resequencing and copy-number detection.Combining microarray-based genomic selection (MGS) with the Illumina Genome Analyzer platform to sequence diploid target regions.Detection of genomic variation by selection of a 9 mb DNA region and high throughput sequencing.Improving the efficiency of genomic loci capture using oligonucleotide arrays for high throughput resequencingChallenges of sequencing human genomes.Targeted exon sequencing by in-solution hybrid selection.Pharmacogenetics and personal genomes.SeqAnt: a web service to rapidly identify and annotate DNA sequence variationsMultiplexed direct genomic selection (MDiGS): a pooled BAC capture approach for highly accurate CNV and SNP/INDEL detection.Performance of microarray and liquid based capture methods for target enrichment for massively parallel sequencing and SNP discovery.Targeted deep resequencing of the human cancer genome using next-generation technologies.Targeted sequencing of the human X chromosome exome.ESRRA-C11orf20 is a recurrent gene fusion in serous ovarian carcinoma.High-density nucleosome occupancy map of human chromosome 9p21-22 reveals chromatin organization of the type I interferon gene cluster.Anchored hybrid enrichment for massively high-throughput phylogenomics.Enrichment of genomic DNA for polymorphism detection in a non-model highly polyploid crop plant.High-throughput sequencing of microdissected chromosomal regions.Targeted sequencing of large genomic regions with CATCH-SeqPseudoautosomal region 1 length polymorphism in the human populationTargeted multiplex next-generation sequencing: advances in techniques of mitochondrial and nuclear DNA sequencing for population genomics.Experiences with array-based sequence capture; toward clinical applications.High-resolution nucleosome mapping of targeted regions using BAC-based enrichmentMicroarray oligonucleotide probe designer (MOPeD): A web serviceMultiplex Chromosomal Exome Sequencing Accelerates Identification of ENU-Induced Mutations in the Mouse.BaitFisher: A Software Package for Multispecies Target DNA Enrichment Probe Design.The Holstein Friesian Lethal Haplotype 5 (HH5) Results from a Complete Deletion of TBF1M and Cholesterol Deficiency (CDH) from an ERV-(LTR) Insertion into the Coding Region of APOB.Genomic Methods Take the Plunge: Recent Advances in High-Throughput Sequencing of Marine Mammals.Expanding anchored hybrid enrichment to resolve both deep and shallow relationships within the spider tree of life.Nucleosome mapping across the CFTR locus identifies novel regulatory factors.Nested Patch PCR enables highly multiplexed mutation discovery in candidate genes
P2860
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P2860
description
2005 nî lūn-bûn
@nan
2005 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
Direct genomic selection.
@ast
Direct genomic selection.
@en
Direct genomic selection.
@nl
type
label
Direct genomic selection.
@ast
Direct genomic selection.
@en
Direct genomic selection.
@nl
prefLabel
Direct genomic selection.
@ast
Direct genomic selection.
@en
Direct genomic selection.
@nl
P2093
P2860
P356
P1433
P1476
Direct genomic selection
@en
P2093
Cynthia Helms
Elaine R Mardis
Rose Veile
Stavros Bashiardes
P2860
P2888
P356
10.1038/NMETH0105-63
P577
2005-01-01T00:00:00Z
P5875
P6179
1051721477