Haplotype sorting using human fosmid clone end-sequence pairs.
about
The human Major Histocompatibility Complex as a paradigm in genomics researchTargeted capture and massively parallel sequencing of 12 human exomesDetermination of haplotypes at structurally complex regions using emulsion haplotype fusion PCRRecurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head sizeA systematic survey of loss-of-function variants in human protein-coding genesValidation of rearrangement break points identified by paired-end sequencing in natural populations of Drosophila melanogaster.Nucleotide, cytogenetic and expression impact of the human chromosome 8p23.1 inversion polymorphism.Population genetic inference from genomic sequence variationA 32 kb critical region excluding Y402H in CFH mediates risk for age-related macular degenerationGenomic pathology of SLE-associated copy-number variation at the FCGR2C/FCGR3B/FCGR2B locus.Long span DNA paired-end-tag (DNA-PET) sequencing strategy for the interrogation of genomic structural mutations and fusion-point-guided reconstruction of amplicons.A definitive haplotype map as determined by genotyping duplicated haploid genomes finds a predominant haplotype preference at copy-number variation eventsA comprehensively molecular haplotype-resolved genome of a European individualResolving the breakpoints of the 17q21.31 microdeletion syndrome with next-generation sequencing.Structural diversity and African origin of the 17q21.31 inversion polymorphism.Haplotype specific-sequencing reveals MBL2 association with asymptomatic Plasmodium falciparum infection.Modeling Human Population Separation History Using Physically Phased Genomes.CBF2A-CBF4B genomic region copy numbers alongside the circadian clock play key regulatory mechanisms driving expression of FR-H2 CBFs.Single-molecule analysis of genome rearrangements in cancer.Recent advances in molecular technologies and their application in pathogen detection in foods with particular reference to yersinia.
P2860
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P2860
Haplotype sorting using human fosmid clone end-sequence pairs.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
2008年论文
@zh
2008年论文
@zh-cn
name
Haplotype sorting using human fosmid clone end-sequence pairs.
@en
type
label
Haplotype sorting using human fosmid clone end-sequence pairs.
@en
prefLabel
Haplotype sorting using human fosmid clone end-sequence pairs.
@en
P2093
P2860
P356
P1433
P1476
Haplotype sorting using human fosmid clone end-sequence pairs.
@en
P2093
Bob Fulton
Evan E Eichler
Richard K Wilson
P2860
P304
P356
10.1101/GR.081786.108
P577
2008-10-03T00:00:00Z