Whole-genome haplotyping using long reads and statistical methods.
about
Tracking Strains in the Microbiome: Insights from Metagenomics and ModelsGenetic variation and the de novo assembly of human genomesThe real cost of sequencing: scaling computation to keep pace with data generationHigh-throughput sequencing technologiesGenome assembly from synthetic long read cloudsSynthetic long-read sequencing reveals intraspecies diversity in the human microbiomeAllelicImbalance: an R/bioconductor package for detecting, managing, and visualizing allele expression imbalance data from RNA sequencingReferences for Haplotype Imputation in the Big Data Era.Benchmarking of de novo assembly algorithms for Nanopore data reveals optimal performance of OLC approaches.Extending partial haplotypes to full genome haplotypes using chromosome conformation capture data.Timber! Felling the loblolly pine genomeGenetic-epigenetic interactions in cis: a major focus in the post-GWAS eraIllumina TruSeq synthetic long-reads empower de novo assembly and resolve complex, highly-repetitive transposable elements.Whole-genome haplotyping approaches and genomic medicine.Accurate, multi-kb reads resolve complex populations and detect rare microorganisms.Haplotype-resolved whole-genome sequencing by contiguity-preserving transposition and combinatorial indexing.Genome assembly using Nanopore-guided long and error-free DNA readsInexpensive multiplexed library preparation for megabase-sized genomes.Assembly and diploid architecture of an individual human genome via single-molecule technologies.One Size Doesn't Fit All - RefEditor: Building Personalized Diploid Reference Genome to Improve Read Mapping and Genotype Calling in Next Generation Sequencing Studies.Read clouds uncover variation in complex regions of the human genome.A simple procedure for directly obtaining haplotype sequences of diploid genomescFinder: definition and quantification of multiple haplotypes in a mixed sample.The landscape of genomic imprinting across diverse adult human tissuesComplete haplotype phasing of the MHC and KIR loci with targeted HaploSeq.Chromatin architecture reorganization during stem cell differentiation.Haplotype-Phased Synthetic Long Reads from Short-Read Sequencing.TruSPAdes: barcode assembly of TruSeq synthetic long reads.Haplotyping germline and cancer genomes with high-throughput linked-read sequencingDiscovery of large genomic inversions using long range informationA vast genomic deletion in the C56BL/6 genome affects different genes within the Ifi200 cluster on chromosome 1 and mediates obesity and insulin resistance.CRISPR-CAS9 D10A nickase target-specific fluorescent labeling of double strand DNA for whole genome mapping and structural variation analysis.The genetic basis for ecological adaptation of the Atlantic herring revealed by genome sequencingDroplet barcoding for massively parallel single-molecule deep sequencingAn accurate clone-based haplotyping method by overlapping pool sequencingPremalignant SOX2 overexpression in the fallopian tubes of ovarian cancer patients: Discovery and validation studies.GenomeLaser: fast and accurate haplotyping from pedigree genotypes.Rare variant phasing and haplotypic expression from RNA sequencing with phASERPWHATSHAP: efficient haplotyping for future generation sequencingModeling Human Population Separation History Using Physically Phased Genomes.
P2860
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P2860
Whole-genome haplotyping using long reads and statistical methods.
description
2014 nî lūn-bûn
@nan
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
2014年论文
@zh
2014年论文
@zh-cn
name
Whole-genome haplotyping using long reads and statistical methods.
@en
type
label
Whole-genome haplotyping using long reads and statistical methods.
@en
prefLabel
Whole-genome haplotyping using long reads and statistical methods.
@en
P2093
P2860
P356
P1433
P1476
Whole-genome haplotyping using long reads and statistical methods.
@en
P2093
Dmitry Pushkarev
Michael Kertesz
Michael Snyder
Tim Blauwkamp
Volodymyr Kuleshov
P2860
P2888
P304
P356
10.1038/NBT.2833
P577
2014-02-23T00:00:00Z