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。Human Genome Sequencing Using Unchained Base Reads on Self-Assembling DNA Nanoarrays
Radoje Drmanac et al.
SCIENCE (2010)
U87MG Decoded: The Genomic Sequence of a Cytogenetically Aberrant Human Cancer Cell Line
Michael James Clark et al.
PLOS GENETICS (2010)
Profiling Bladder Cancer Organ Site-Specific Metastasis Identifies LAMC2 as a Novel Biomarker of Hematogenous Dissemination
Steven Christopher Smith et al.
AMERICAN JOURNAL OF PATHOLOGY (2009)
Fast and accurate short read alignment with Burrows-Wheeler transform
Heng Li et al.
BIOINFORMATICS (2009)
Sequence diversity in three tomato species: SNPs, markers, and molecular evolution
Jose M. Jimenez-Gomez et al.
BMC PLANT BIOLOGY (2009)
The N-Myc-DLL3 Cascade Is Suppressed by the Ubiquitin Ligase Huwe1 to Inhibit Proliferation and Promote Neurogenesis in the Developing Brain
Xudong Zhao et al.
DEVELOPMENTAL CELL (2009)
The consensus coding sequence (CCDS) project: Identifying a common protein-coding gene set for the human and mouse genomes
Kim D. Pruitt et al.
GENOME RESEARCH (2009)
Sequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encoding
Kevin Judd McKernan et al.
GENOME RESEARCH (2009)
Targeted capture and massively parallel sequencing of 12 human exomes
Sarah B. Ng et al.
NATURE (2009)
Common Genetic Variation and Human Traits
David B. Goldstein
NEW ENGLAND JOURNAL OF MEDICINE (2009)
Ultrafast and memory-efficient alignment of short DNA sequences to the human genome
Ben Langmead et al.
GENOME BIOLOGY (2009)
SOAP: short oligonucleotide alignment program
Ruiqiang Li et al.
BIOINFORMATICS (2008)
Overexpression of CDC25B and LAMC2 mRNA and protein in esophageal squamous cell carcinomas and premalignant lesions in subjects from a high-risk population in China
Jian-Zhong Shou et al.
CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION (2008)
The diploid genome sequence of an Asian individual
Jun Wang et al.
NATURE (2008)
Accurate whole human genome sequencing using reversible terminator chemistry
David R. Bentley et al.
NATURE (2008)
Genome-wide association studies for complex traits: consensus, uncertainty and challenges
Mark I. McCarthy et al.
NATURE REVIEWS GENETICS (2008)
Genetic Variation in an Individual Human Exome
Pauline C. Ng et al.
PLOS GENETICS (2008)
The diploid genome sequence of an individual human
Samuel Levy et al.
PLOS BIOLOGY (2007)
Common sequence polymorphisms shaping genetic diversity in Arabidopsis thaliana
Richard M. Clark et al.
SCIENCE (2007)
A silent polymorphism in the MDR1 gene changes substrate specificity
Chava Kimchi-Sarfaty et al.
SCIENCE (2007)
The UCSC Genome Browser Database: Update 2007
R. M. Kuhn et al.
NUCLEIC ACIDS RESEARCH (2007)
An initial map of insertion and deletion (INDEL) variation in the human genome
Ryan E. Mills et al.
GENOME RESEARCH (2006)
Applications for protein sequence-function evolution data: mRNA/protein expression analysis and coding SNP scoring tools
Paul D. Thomas et al.
NUCLEIC ACIDS RESEARCH (2006)
Genetically distinct and clinically relevant subtypes of glioblastoma defined by array-based comparative genomic hybridization (array-CGH)
A Korshunov et al.
ACTA NEUROPATHOLOGICA (2006)
Complement factor H polymorphism in age-related macular degeneration
RJ Klein et al.
SCIENCE (2005)
Whole-genome patterns of common DNA variation in three human populations
DA Hinds et al.
SCIENCE (2005)
Repbase update, a database of eukaryotic repetitive elements
J Jurka et al.
CYTOGENETIC AND GENOME RESEARCH (2005)
Modeling of DNA microarray data by using physical properties of hybridization
GA Held et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2003)
Synonymous mutations in the human dopamine receptor D2 (DRD2) affect mRNA stability and synthesis of the receptor
JB Duan et al.
HUMAN MOLECULAR GENETICS (2003)
Human non-synonymous SNPs: server and survey
V Ramensky et al.
NUCLEIC ACIDS RESEARCH (2002)
Accounting for human polymorphisms predicted to affect protein function
PC Ng et al.
GENOME RESEARCH (2002)
Gene-based SNP discovery as part of the Japanese Millennium Genome Project: identification of 190562 genetic variations in the human genome
H Haga et al.
JOURNAL OF HUMAN GENETICS (2002)
Large-scale discovery and genotyping of single-nucleotide polymorphisms in the mouse
K Lindblad-Toh et al.
NATURE GENETICS (2000)