相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。TranslatomeDB: a comprehensive database and cloud-based analysis platform for translatome sequencing data
Wanting Liu et al.
NUCLEIC ACIDS RESEARCH (2018)
Optimal Settings of Mass Spectrometry Open Search Strategy for Higher Confidence
Dehua Li et al.
JOURNAL OF PROTEOME RESEARCH (2018)
Evaluation of GRCh38 and de novo haploid genome assemblies demonstrates the enduring quality of the reference assembly
Valerie A. Schneider et al.
GENOME RESEARCH (2017)
MECAT : fast mapping, error correction, and de novo assembly for single-molecule sequencing reads
Chuan-Le Xiao et al.
NATURE METHODS (2017)
Low-cost, Low-bias and Low-input RNA-seq with High Experimental Verifiability based on Semiconductor Sequencing
Zhibiao Mai et al.
SCIENTIFIC REPORTS (2017)
Data Descriptor: 11,670 whole-genome sequences representative of the Han Chinese population from the CONVERGE project
Na Cai et al.
SCIENTIFIC DATA (2017)
10 Years of GWAS Discovery: Biology, Function, and Translation
Peter M. Visscher et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2017)
An ethnically relevant consensus Korean reference genome is a step towards personal reference genomes
Yun Sung Cho et al.
NATURE COMMUNICATIONS (2016)
Long-read sequencing and de novo assembly of a Chinese genome
Lingling Shi et al.
NATURE COMMUNICATIONS (2016)
A global reference for human genetic variation
David M. Altshuler et al.
NATURE (2015)
EPITHELIAL SODIUM TRANSPORT AND ITS CONTROL BY ALDOSTERONE: THE STORY OF OUR INTERNAL ENVIRONMENT REVISITED
Bernard C. Rossier et al.
PHYSIOLOGICAL REVIEWS (2015)
Iterative Genome Correction Largely Improves Proteomic Analysis of Nonmodel Organisms
Xiaohui Wu et al.
JOURNAL OF PROTEOME RESEARCH (2014)
The genomic landscape of polymorphic human nuclear mitochondrial insertions
Gargi Dayama et al.
NUCLEIC ACIDS RESEARCH (2014)
FANSe2: A Robust and Cost-Efficient Alignment Tool for Quantitative Next-Generation Sequencing Applications
Chuan-Le Xiao et al.
PLOS ONE (2014)
A survey of error-correction methods for next-generation sequencing
Xiao Yang et al.
BRIEFINGS IN BIOINFORMATICS (2013)
Rapid, economical single-nucleotide polymorphism and microsatellite discovery based on de novo assembly of a reduced representation genome in a non-model organism: a case study of Atlantic cod Gadus morhua
J. Carlsson et al.
JOURNAL OF FISH BIOLOGY (2013)
Single-cell sequencing-based technologies will revolutionize whole-organism science
Ehud Shapiro et al.
NATURE REVIEWS GENETICS (2013)
Translating mRNAs strongly correlate to proteins in a multivariate manner and their translation ratios are phenotype specific
Tong Wang et al.
NUCLEIC ACIDS RESEARCH (2013)
An integrated map of genetic variation from 1,092 human genomes
David M. Altshuler et al.
NATURE (2012)
FANSe: an accurate algorithm for quantitative mapping of large scale sequencing reads
Gong Zhang et al.
NUCLEIC ACIDS RESEARCH (2012)
Rank and Order: Evaluating the Performance of SNPs for Individual Assignment in a Non-Model Organism
Caroline G. Storer et al.
PLOS ONE (2012)
Genetic architecture of cancer and other complex diseases: lessons learned and future directions
Lucia A. Hindorff et al.
CARCINOGENESIS (2011)
High-quality draft assemblies of mammalian genomes from massively parallel sequence data
Sante Gnerre et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2011)
De novo assembly of human genomes with massively parallel short read sequencing
Ruiqiang Li et al.
GENOME RESEARCH (2010)
Measuring differential gene expression by short read sequencing: quantitative comparison to 2-channel gene expression microarrays
Joshua S. Bloom et al.
BMC GENOMICS (2009)
Real-Time DNA Sequencing from Single Polymerase Molecules
John Eid et al.
SCIENCE (2009)
The diploid genome sequence of an Asian individual
Jun Wang et al.
NATURE (2008)
Mapping and quantifying mammalian transcriptomes by RNA-Seq
Ali Mortazavi et al.
NATURE METHODS (2008)
Genome-wide association studies for complex traits: consensus, uncertainty and challenges
Mark I. McCarthy et al.
NATURE REVIEWS GENETICS (2008)
Mitochondrial DNA-like sequences in the nucleus (NUMTs): Insights into our African origins and the mechanism of foreign DNA integration
D Mishmar et al.
HUMAN MUTATION (2004)
Initial sequencing and analysis of the human genome
ES Lander et al.
NATURE (2001)