Resolving the complexity of the human genome using single-molecule sequencing - Test2 - elhamkhani - TriplyDB

Resolving the complexity of the human genome using single-molecule sequencing

Resolving the complexity of the human genome using single-molecule sequencing

http://www.wikidata.org/entity/Q22122132

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Medical implications of technical accuracy in genome sequencing A global reference for human genetic variation Palindrome-Mediated Translocations in Humans: A New Mechanistic Model for Gross Chromosomal Rearrangements Unraveling the message: insights into comparative genomics of the naked mole-rat Transposable element detection from whole genome sequence data Analysis of single nucleic acid molecules in micro- and nano-fluidics Cracking the Code of Human Diseases Using Next-Generation Sequencing: Applications, Challenges, and Perspectives PacBio Sequencing and Its Applications Next-Generation Sequencing Approaches in Cancer: Where Have They Brought Us and Where Will They Take Us?Next-Generation Sequencing in Clinical Molecular Diagnostics of Cancer: Advantages and Challenges Genetic variation and the de novo assembly of human genomes Structural variation discovery in the cancer genome using next generation sequencing: computational solutions and perspectives Omics-Based Strategies in Precision Medicine: Toward a Paradigm Shift in Inborn Errors of Metabolism Investigations Oxford Nanopore MinION Sequencing and Genome Assembly New insights into the generation and role of de novo mutations in health and disease The genetic heterogeneity of colorectal cancer predisposition - guidelines for gene discovery Detection of Genomic Structural Variants from Next-Generation Sequencing Data A genome-wide approach for detecting novel insertion-deletion variants of mid-range size L1Base 2: more retrotransposition-active LINE-1s, more mammalian genomes BioNano genome mapping of individual chromosomes supports physical mapping and sequence assembly in complex plant genomes Chromosomal-Level Assembly of the Asian Seabass Genome Using Long Sequence Reads and Multi-layered Scaffolding Genomic DNA transposition induced by human PGBD5 High-throughput sequencing technologies Genome assembly from synthetic long read clouds Comparative analyses of the major royal jelly protein gene cluster in three Apis species with long amplicon sequencing.A hybrid approach for de novo human genome sequence assembly and phasing.Hybrid sequencing and map finding (HySeMaFi): optional strategies for extensively deciphering gene splicing and expression in organisms without reference genome Genomic structure of the horse major histocompatibility complex class II region resolved using PacBio long-read sequencing technology.Accurate typing of short tandem repeats from genome-wide sequencing data and its applications.Detecting non-allelic homologous recombination from high-throughput sequencing data.Biological data sciences in genome research.A new molecular signature method for prediction of driver cancer pathways from transcriptional data.Benchmarking of de novo assembly algorithms for Nanopore data reveals optimal performance of OLC approaches.Improve homology search sensitivity of PacBio data by correcting frameshifts.Rapid Evolutionary Rates and Unique Genomic Signatures Discovered in the First Reference Genome for the Southern Ocean Salp, Salpa thompsoni (Urochordata, Thaliacea)From next-generation resequencing reads to a high-quality variant data set.The combination of direct and paired link graphs can boost repetitive genome assembly.Genome graphs and the evolution of genome inference Single-molecule sequencing resolves the detailed structure of complex satellite DNA loci in Drosophila melanogaster ABySS 2.0: resource-efficient assembly of large genomes using a Bloom filter.

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Resolving the complexity of the human genome using single-molecule sequencing

http://www.wikidata.org/entity/Q22122132

description

2015 nî lūn-bûn

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2015 թուականի Յունուարին հրատարակուած գիտական յօդուած

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2015 թվականի հունվարին հրատարակված գիտական հոդված

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2015年の論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年论文

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name

Resolving the complexity of the human genome using single-molecule sequencing

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Resolving the complexity of the human genome using single-molecule sequencing

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Resolving the complexity of the human genome using single-molecule sequencing

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Resolving the complexity of the human genome using single-molecule sequencing

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Resolving the complexity of the human genome using single-molecule sequencing

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Resolving the complexity of the human genome using single-molecule sequencing

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Resolving the complexity of the human genome using single-molecule sequencing

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Resolving the complexity of the human genome using single-molecule sequencing

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Resolving the complexity of the human genome using single-molecule sequencing

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Resolving the complexity of the human genome using single-molecule sequencing

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Resolving the complexity of the human genome using single-molecule sequencing

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Resolving the complexity of the human genome using single-molecule sequencing

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Resolving the complexity of the human genome using single-molecule sequencing

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John Huddleston

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Maika Malig

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Urvashi Surti

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Initial sequencing and analysis of the human genome

The Sequence of the Human Genome

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

Finishing the euchromatic sequence of the human genome

A vast collection of microbial genes that are toxic to bacteria

Mapping copy number variation by population-scale genome sequencing

The International HapMap Project

Real-time DNA sequencing from single polymerase molecules

Origins and functional impact of copy number variation in the human genome

A high-resolution recombination map of the human genome

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10.1038/NATURE13907

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Fereydoun Hormozdiari

Matthew Boitano

Peter H Sudmant

Francesca Antonacci

Richard Sandstrom

Evan E. Eichler

John A Stamatoyannopoulos

Michael W. Hunkapiller

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2015-01-29T00:00:00Z

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