Chromosomal haplotypes by genetic phasing of human families
about
Relationship estimation from whole-genome sequence dataPromise of personalized omics to precision medicineVariations in brain DNASequence to Medical Phenotypes: A Framework for Interpretation of Human Whole Genome DNA Sequence DataCrowdsourced direct-to-consumer genomic analysis of a family quartetOdintifier--A computational method for identifying insertions of organellar origin from modern and ancient high-throughput sequencing data based on haplotype phasingX-linked MTMR8 diversity and evolutionary history of sub-Saharan populationsDetermination of haplotypes at structurally complex regions using emulsion haplotype fusion PCRAn EM algorithm based on an internal list for estimating haplotype distributions of rare variants from pooled genotype dataFamSeq: a variant calling program for family-based sequencing data using graphics processing units.Phased diploid genome assembly with single-molecule real-time sequencing.Imputation in families using a heuristic phasing approach.Growing up in the genomic era: implications of whole-genome sequencing for children, families, and pediatric practice.Accurate whole-genome sequencing and haplotyping from 10 to 20 human cells.A fast collapsed data method for estimating haplotype frequencies from pooled genotype data with applications to the study of rare variants.Whole-genome haplotyping approaches and genomic medicine.Fine-scale mapping of meiotic recombination in AsiansComplete genome phasing of family quartet by combination of genetic, physical and population-based phasing analysisAccurate and robust prediction of genetic relationship from whole-genome sequences.Detection and phasing of single base de novo mutations in biopsies from human in vitro fertilized embryos by advanced whole-genome sequencingDominant sequences of human major histocompatibility complex conserved extended haplotypes from HLA-DQA2 to DAXXHaplotyping germline and cancer genomes with high-throughput linked-read sequencingRecombination mapping using Boolean logic and high-density SNP genotyping for exome sequence filtering.Rare variant detection using family-based sequencing analysisRare variant phasing and haplotypic expression from RNA sequencing with phASERSystems approaches to biology and disease enable translational systems medicine.Systems biology and p4 medicine: past, present, and future.Read-based phasing of related individuals.Mutations in STX1B, encoding a presynaptic protein, cause fever-associated epilepsy syndromes.Whole-genome haplotyping using long reads and statistical methods.Phased Genome Sequencing Through Chromosome Sorting.
P2860
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P2860
Chromosomal haplotypes by genetic phasing of human families
description
2011 nî lūn-bûn
@nan
2011 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
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
name
Chromosomal haplotypes by genetic phasing of human families
@ast
Chromosomal haplotypes by genetic phasing of human families
@en
Chromosomal haplotypes by genetic phasing of human families
@nl
type
label
Chromosomal haplotypes by genetic phasing of human families
@ast
Chromosomal haplotypes by genetic phasing of human families
@en
Chromosomal haplotypes by genetic phasing of human families
@nl
prefLabel
Chromosomal haplotypes by genetic phasing of human families
@ast
Chromosomal haplotypes by genetic phasing of human families
@en
Chromosomal haplotypes by genetic phasing of human families
@nl
P2093
P2860
P50
P3181
P1476
Chromosomal haplotypes by genetic phasing of human families
@en
P2093
Alisha K Holloway
Arian F A Smit
David J Galas
Deepak Srivastava
Denise E Mauldin
Jared C Roach
Katherine S Pollard
Robert Hubley
Stephen Z Montsaroff
P2860
P304
P3181
P356
10.1016/J.AJHG.2011.07.023
P407
P577
2011-09-09T00:00:00Z