Haplotyping germline and cancer genomes with high-throughput linked-read sequencing - Wikidata - awgldk - TriplyDB

Haplotyping germline and cancer genomes with high-throughput linked-read sequencing

Haplotyping germline and cancer genomes with high-throughput linked-read sequencing

http://www.wikidata.org/entity/Q35909792

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Omics-Based Strategies in Precision Medicine: Toward a Paradigm Shift in Inborn Errors of Metabolism Investigations A hybrid approach for de novo human genome sequence assembly and phasing.Massively parallel digital transcriptional profiling of single cells A reference data set of 5.4 million phased human variants validated by genetic inheritance from sequencing a three-generation 17-member pedigree.Using reference-free compressed data structures to analyze sequencing reads from thousands of human genomes Canu: scalable and accurate long-read assembly via adaptive k-mer weighting and repeat separation.Human Y chromosome copy number variation in the next generation sequencing era and beyond.Sequencing and de novo assembly of a near complete indica rice genome.Genome annotation for clinical genomic diagnostics: strengths and weaknesses de novo assembly and population genomic survey of natural yeast isolates with the Oxford Nanopore MinION sequencer.New Cancer Immunotherapy Agents in Development: a report from an associated program of the 31stAnnual Meeting of the Society for Immunotherapy of Cancer, 2016 Linked read sequencing resolves complex genomic rearrangements in gastric cancer metastases.Integrative analysis of genomic alterations in triple-negative breast cancer in association with homologous recombination deficiency.Scaffolding of long read assemblies using long range contact information.Optical DNA mapping in nanofluidic devices: principles and applications.A method for high-throughput production of sequence-verified DNA libraries and strain collections.Defining the diverse spectrum of inversions, complex structural variation, and chromothripsis in the morbid human genome.Direct determination of diploid genome sequences.Droplet Barcode Sequencing for targeted linked-read haplotyping of single DNA molecules.Droplet barcoding for massively parallel single-molecule deep sequencing Exome-based Variant Detection in Core Promoters Allele-Specific Quantification of Structural Variations in Cancer Genomes.Genome-wide characteristics of de novo mutations in autism Abseq: Ultrahigh-throughput single cell protein profiling with droplet microfluidic barcoding.Reference standards for next-generation sequencing.Genome-wide reconstruction of complex structural variants using read clouds.Advances in Decoding Axolotl Limb Regeneration.Genetic Approaches to Understanding Psychiatric Disease.Genomic innovation for crop improvement.The Y chromosomes of the great apes.Computational pan-genomics: status, promises and challenges.BCFtools/csq: haplotype-aware variant consequences.HapCUT2: robust and accurate haplotype assembly for diverse sequencing technologies.Extraction of High Molecular Weight DNA from Fungal Rust Spores for Long Read Sequencing.Noninvasive prenatal diagnosis of 21-Hydroxylase deficiency using target capture sequencing of maternal plasma DNA.Comprehensive comparison of Pacific Biosciences and Oxford Nanopore Technologies and their applications to transcriptome analysis.Direct chromosome-length haplotyping by single-cell sequencing.Recent Advances in Experimental Whole Genome Haplotyping Methods.The context of prostate cancer genomics in personalized medicine.The Apostasia genome and the evolution of orchids.

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Haplotyping germline and cancer genomes with high-throughput linked-read sequencing

http://www.wikidata.org/entity/Q35909792

description

2016 nî lūn-bûn

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2016年の論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年论文

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2016年论文

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2016年论文

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name

Haplotyping germline and cancer genomes with high-throughput linked-read sequencing

@ast

Haplotyping germline and cancer genomes with high-throughput linked-read sequencing

@en

type

label

Haplotyping germline and cancer genomes with high-throughput linked-read sequencing

@ast

Haplotyping germline and cancer genomes with high-throughput linked-read sequencing

@en

prefLabel

Haplotyping germline and cancer genomes with high-throughput linked-read sequencing

@ast

Haplotyping germline and cancer genomes with high-throughput linked-read sequencing

@en

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P1433

Nature Biotechnology

P1476

Haplotyping germline and cancer genomes with high-throughput linked-read sequencing

@en

P2093

Adam J Lowe

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Adrian Chan

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Adrian N Fehr

http://www.w3.org/2001/XMLSchema#string

Alex Kindwall

http://www.w3.org/2001/XMLSchema#string

Alexander Wong

http://www.w3.org/2001/XMLSchema#string

Andrew D Price

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Anthony J Makarewicz

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Benjamin J Hindson

http://www.w3.org/2001/XMLSchema#string

Billy T Lau

http://www.w3.org/2001/XMLSchema#string

Christina Wood

http://www.w3.org/2001/XMLSchema#string

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Gene copy-number polymorphism caused by retrotransposition in humans

LUMPY: a probabilistic framework for structural variant discovery.

An integrated map of genetic variation from 1,092 human genomes

Mapping and sequencing of structural variation from eight human genomes

Chromosomal haplotypes by genetic phasing of human families

Mapping copy number variation by population-scale genome sequencing

Comprehensive molecular characterization of human colon and rectal cancer

The haplotype-resolved genome and epigenome of the aneuploid HeLa cancer cell line

Identification of the transforming EML4-ALK fusion gene in non-small-cell lung cancer.

Identification of novel isoforms of the EML4-ALK transforming gene in non-small cell lung cancer.

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303-311

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scholarly article

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10.1038/NBT.3432

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3

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34

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Glenn K Lockwood

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2016-02-01T00:00:00Z

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292670765

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26829319

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4786454

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