-
ChIP-seq guidelines and practices of the ENCODE and modENCODE consortia.
Genome Res. 2012 Sep;22(9):1813-31
PMID: 22955991
-
Exploring the three-dimensional organization of genomes: interpreting chromatin interaction data.
Nat Rev Genet. 2013 Jun;14(6):390-403
PMID: 23657480
-
ChIP-seq: advantages and challenges of a maturing technology.
Nat Rev Genet. 2009 Oct;10(10):669-80
PMID: 19736561
-
Efficient study design for next generation sequencing.
Genet Epidemiol. 2011 May;35(4):269-77
PMID: 21370254
-
An initial strategy for the systematic identification of functional elements in the human genome by low-redundancy comparative sequencing.
Proc Natl Acad Sci U S A. 2005 Mar 29;102(13):4795-800
PMID: 15778292
-
Assembly of large genomes using second-generation sequencing.
Genome Res. 2010 Sep;20(9):1165-73
PMID: 20508146
-
Fast computation and applications of genome mappability.
PLoS One. 2012;7(1):e30377
PMID: 22276185
-
Benchmarking short sequence mapping tools.
BMC Bioinformatics. 2013 Jun 07;14:184
PMID: 23758764
-
A Bayesian deconvolution strategy for immunoprecipitation-based DNA methylome analysis.
Nat Biotechnol. 2008 Jul;26(7):779-85
PMID: 18612301
-
A hypermorphic missense mutation in PLCG2, encoding phospholipase Cγ2, causes a dominantly inherited autoinflammatory disease with immunodeficiency.
Am J Hum Genet. 2012 Oct 5;91(4):713-20
PMID: 23000145
-
Comprehensive genome-wide protein-DNA interactions detected at single-nucleotide resolution.
Cell. 2011 Dec 9;147(6):1408-19
PMID: 22153082
-
Methylome analysis using MeDIP-seq with low DNA concentrations.
Nat Protoc. 2012 Mar 08;7(4):617-36
PMID: 22402632
-
Discovery and statistical genotyping of copy-number variation from whole-exome sequencing depth.
Am J Hum Genet. 2012 Oct 5;91(4):597-607
PMID: 23040492
-
Robust 4C-seq data analysis to screen for regulatory DNA interactions.
Nat Methods. 2012 Oct;9(10):969-72
PMID: 22961246
-
Differential expression in RNA-seq: a matter of depth.
Genome Res. 2011 Dec;21(12):2213-23
PMID: 21903743
-
Sequence assembly demystified.
Nat Rev Genet. 2013 Mar;14(3):157-67
PMID: 23358380
-
Bio-CAP: a versatile and highly sensitive technique to purify and characterise regions of non-methylated DNA.
Nucleic Acids Res. 2012 Feb;40(4):e32
PMID: 22156374
-
Global mapping of protein-DNA interactions in vivo by digital genomic footprinting.
Nat Methods. 2009 Apr;6(4):283-9
PMID: 19305407
-
ChIA-PET analysis of transcriptional chromatin interactions.
Methods. 2012 Nov;58(3):289-99
PMID: 22926262
-
Integrative annotation of human large intergenic noncoding RNAs reveals global properties and specific subclasses.
Genes Dev. 2011 Sep 15;25(18):1915-27
PMID: 21890647
-
A likelihood-based framework for variant calling and de novo mutation detection in families.
PLoS Genet. 2012;8(10):e1002944
PMID: 23055937
-
CNV-seq, a new method to detect copy number variation using high-throughput sequencing.
BMC Bioinformatics. 2009 Mar 06;10:80
PMID: 19267900
-
An integrated map of genetic variation from 1,092 human genomes.
Nature. 2012 Nov 1;491(7422):56-65
PMID: 23128226
-
LIN28A is a suppressor of ER-associated translation in embryonic stem cells.
Cell. 2012 Nov 9;151(4):765-777
PMID: 23102813
-
The mutation spectrum revealed by paired genome sequences from a lung cancer patient.
Nature. 2010 May 27;465(7297):473-7
PMID: 20505728
-
Differential analysis of gene regulation at transcript resolution with RNA-seq.
Nat Biotechnol. 2013 Jan;31(1):46-53
PMID: 23222703
-
A global view of gene activity and alternative splicing by deep sequencing of the human transcriptome.
Science. 2008 Aug 15;321(5891):956-60
PMID: 18599741
-
Splicing factor SFRS1 recognizes a functionally diverse landscape of RNA transcripts.
Genome Res. 2009 Mar;19(3):381-94
PMID: 19116412
-
A comprehensive comparison of RNA-Seq-based transcriptome analysis from reads to differential gene expression and cross-comparison with microarrays: a case study in Saccharomyces cerevisiae.
Nucleic Acids Res. 2012 Nov 1;40(20):10084-97
PMID: 22965124
-
Evaluation of statistical methods for normalization and differential expression in mRNA-Seq experiments.
BMC Bioinformatics. 2010 Feb 18;11:94
PMID: 20167110
-
Performance comparison of exome DNA sequencing technologies.
Nat Biotechnol. 2011 Sep 25;29(10):908-14
PMID: 21947028
-
HITS-CLIP yields genome-wide insights into brain alternative RNA processing.
Nature. 2008 Nov 27;456(7221):464-9
PMID: 18978773
-
Finished bacterial genomes from shotgun sequence data.
Genome Res. 2012 Nov;22(11):2270-7
PMID: 22829535
-
Widespread binding of FUS along nascent RNA regulates alternative splicing in the brain.
Sci Rep. 2012;2:603
PMID: 22934129
-
How deep is deep enough for RNA-Seq profiling of bacterial transcriptomes?
BMC Genomics. 2012 Dec 27;13:734
PMID: 23270466
-
A large genome center's improvements to the Illumina sequencing system.
Nat Methods. 2008 Dec;5(12):1005-10
PMID: 19034268
-
Determining long-range chromatin interactions for selected genomic sites using 4C-seq technology: from fixation to computation.
Methods. 2012 Nov;58(3):221-30
PMID: 22609568
-
Genome-wide transcription and the implications for genomic organization.
Nat Rev Genet. 2007 Jun;8(6):413-23
PMID: 17486121
-
Predicting the molecular complexity of sequencing libraries.
Nat Methods. 2013 Apr;10(4):325-7
PMID: 23435259
-
From cells to chromatin: capturing snapshots of genome organization with 5C technology.
Methods. 2012 Nov;58(3):255-67
PMID: 23137922
-
The GENCODE v7 catalog of human long noncoding RNAs: analysis of their gene structure, evolution, and expression.
Genome Res. 2012 Sep;22(9):1775-89
PMID: 22955988
-
ChIP-exo method for identifying genomic location of DNA-binding proteins with near-single-nucleotide accuracy.
Curr Protoc Mol Biol. 2012 Oct;Chapter 21:Unit 21.24
PMID: 23026909
-
Exome RNA sequencing reveals rare and novel alternative transcripts.
Nucleic Acids Res. 2013 Jan 7;41(1):e6
PMID: 22941640
-
SNP detection and genotyping from low-coverage sequencing data on multiple diploid samples.
Genome Res. 2011 Jun;21(6):952-60
PMID: 20980557
-
3C-based technologies to study the shape of the genome.
Methods. 2012 Nov;58(3):189-91
PMID: 23199640
-
Current challenges in de novo plant genome sequencing and assembly.
Genome Biol. 2012;13(4):243
PMID: 22546054
-
Design and analysis of ChIP-seq experiments for DNA-binding proteins.
Nat Biotechnol. 2008 Dec;26(12):1351-9
PMID: 19029915
-
PeakSeq enables systematic scoring of ChIP-seq experiments relative to controls.
Nat Biotechnol. 2009 Jan;27(1):66-75
PMID: 19122651
-
Insights into the evolution of Darwin's finches from comparative analysis of the Geospiza magnirostris genome sequence.
BMC Genomics. 2013 Feb 12;14:95
PMID: 23402223
-
Alternative isoform regulation in human tissue transcriptomes.
Nature. 2008 Nov 27;456(7221):470-6
PMID: 18978772
-
Viral microRNA targetome of KSHV-infected primary effusion lymphoma cell lines.
Cell Host Microbe. 2011 Nov 17;10(5):515-26
PMID: 22100165
-
The first Korean genome sequence and analysis: full genome sequencing for a socio-ethnic group.
Genome Res. 2009 Sep;19(9):1622-9
PMID: 19470904
-
cn.MOPS: mixture of Poissons for discovering copy number variations in next-generation sequencing data with a low false discovery rate.
Nucleic Acids Res. 2012 May;40(9):e69
PMID: 22302147
-
Genomic mapping by fingerprinting random clones: a mathematical analysis.
Genomics. 1988 Apr;2(3):231-9
PMID: 3294162
-
Hi-C: a comprehensive technique to capture the conformation of genomes.
Methods. 2012 Nov;58(3):268-76
PMID: 22652625
-
High-throughput microbial population genomics using the Cortex variation assembler.
Bioinformatics. 2013 Jan 15;29(2):275-6
PMID: 23172865
-
A framework for variation discovery and genotyping using next-generation DNA sequencing data.
Nat Genet. 2011 May;43(5):491-8
PMID: 21478889
-
NOVA-dependent regulation of cryptic NMD exons controls synaptic protein levels after seizure.
Elife. 2013 Jan 22;2:e00178
PMID: 23359859
-
Next generation sequencing has lower sequence coverage and poorer SNP-detection capability in the regulatory regions.
Sci Rep. 2011;1:55
PMID: 22355574
-
Low-coverage sequencing: implications for design of complex trait association studies.
Genome Res. 2011 Jun;21(6):940-51
PMID: 21460063
-
Epigenetic conservation at gene regulatory elements revealed by non-methylated DNA profiling in seven vertebrates.
Elife. 2013 Feb 26;2:e00348
PMID: 23467541
-
The sequence and de novo assembly of the giant panda genome.
Nature. 2010 Jan 21;463(7279):311-7
PMID: 20010809
-
The diploid genome sequence of an Asian individual.
Nature. 2008 Nov 6;456(7218):60-5
PMID: 18987735
-
Differential expression analysis for sequence count data.
Genome Biol. 2010;11(10):R106
PMID: 20979621
-
The genome sequence of the colonial chordate, Botryllus schlosseri.
Elife. 2013 Jul 02;2:e00569
PMID: 23840927
-
The transcriptional landscape of the yeast genome defined by RNA sequencing.
Science. 2008 Jun 6;320(5881):1344-9
PMID: 18451266
-
RNA-Seq: a revolutionary tool for transcriptomics.
Nat Rev Genet. 2009 Jan;10(1):57-63
PMID: 19015660
-
edgeR: a Bioconductor package for differential expression analysis of digital gene expression data.
Bioinformatics. 2010 Jan 1;26(1):139-40
PMID: 19910308
-
Assemblathon 2: evaluating de novo methods of genome assembly in three vertebrate species.
Gigascience. 2013 Jul 22;2(1):10
PMID: 23870653
-
TopHat: discovering splice junctions with RNA-Seq.
Bioinformatics. 2009 May 1;25(9):1105-11
PMID: 19289445
-
Comprehensive comparison of three commercial human whole-exome capture platforms.
Genome Biol. 2011 Sep 28;12(9):R95
PMID: 21955857
-
Accurate whole human genome sequencing using reversible terminator chemistry.
Nature. 2008 Nov 6;456(7218):53-9
PMID: 18987734
-
Copy number variation detection and genotyping from exome sequence data.
Genome Res. 2012 Aug;22(8):1525-32
PMID: 22585873
-
Transcriptome-wide identification of RNA-binding protein and microRNA target sites by PAR-CLIP.
Cell. 2010 Apr 2;141(1):129-41
PMID: 20371350
-
Biases in Illumina transcriptome sequencing caused by random hexamer priming.
Nucleic Acids Res. 2010 Jul;38(12):e131
PMID: 20395217
-
Genomic maps of long noncoding RNA occupancy reveal principles of RNA-chromatin interactions.
Mol Cell. 2011 Nov 18;44(4):667-78
PMID: 21963238
-
Aegilops tauschii draft genome sequence reveals a gene repertoire for wheat adaptation.
Nature. 2013 Apr 4;496(7443):91-5
PMID: 23535592
-
Monitoring chronic lymphocytic leukemia progression by whole genome sequencing reveals heterogeneous clonal evolution patterns.
Blood. 2012 Nov 15;120(20):4191-6
PMID: 22915640
-
Genome-wide structure and organization of eukaryotic pre-initiation complexes.
Nature. 2012 Jan 18;483(7389):295-301
PMID: 22258509
-
Comparison of solution-based exome capture methods for next generation sequencing.
Genome Biol. 2011 Sep 28;12(9):R94
PMID: 21955854
-
Initial sequencing and analysis of the human genome.
Nature. 2001 Feb 15;409(6822):860-921
PMID: 11237011
-
2x genomes--does depth matter?
Genome Res. 2007 Nov;17(11):1547-9
PMID: 17975171
-
Amplification-free Illumina sequencing-library preparation facilitates improved mapping and assembly of (G+C)-biased genomes.
Nat Methods. 2009 Apr;6(4):291-5
PMID: 19287394
-
Analyzing and minimizing PCR amplification bias in Illumina sequencing libraries.
Genome Biol. 2011;12(2):R18
PMID: 21338519
-
Proposed methods for testing and selecting the ERCC external RNA controls.
BMC Genomics. 2005 Nov 02;6:150
PMID: 16266432
-
Detecting copy number variation with mated short reads.
Genome Res. 2010 Nov;20(11):1613-22
PMID: 20805290
-
mRNA expression, splicing and editing in the embryonic and adult mouse cerebral cortex.
Nat Neurosci. 2013 Apr;16(4):499-506
PMID: 23416452
-
Genome-wide mapping of in vivo protein-DNA interactions.
Science. 2007 Jun 8;316(5830):1497-502
PMID: 17540862
-
Systematic evaluation of factors influencing ChIP-seq fidelity.
Nat Methods. 2012 Jun;9(6):609-14
PMID: 22522655
-
GAGE: A critical evaluation of genome assemblies and assembly algorithms.
Genome Res. 2012 Mar;22(3):557-67
PMID: 22147368
-
High resolution mapping of Twist to DNA in Drosophila embryos: Efficient functional analysis and evolutionary conservation.
Genome Res. 2011 Apr;21(4):566-77
PMID: 21383317
-
Extremely low-coverage sequencing and imputation increases power for genome-wide association studies.
Nat Genet. 2012 May 20;44(6):631-5
PMID: 22610117
-
The ENCODE (ENCyclopedia Of DNA Elements) Project.
Science. 2004 Oct 22;306(5696):636-40
PMID: 15499007
-
Accurate and comprehensive sequencing of personal genomes.
Genome Res. 2011 Sep;21(9):1498-505
PMID: 21771779
-
A streamlined method for detecting structural variants in cancer genomes by short read paired-end sequencing.
PLoS One. 2012;7(10):e48314
PMID: 23144753
-
A mechanistic basis for amplification differences between samples and between genome regions.
BMC Genomics. 2012 Sep 05;13:455
PMID: 22950736
-
The long-range interaction landscape of gene promoters.
Nature. 2012 Sep 6;489(7414):109-13
PMID: 22955621
-
iCLIP reveals the function of hnRNP particles in splicing at individual nucleotide resolution.
Nat Struct Mol Biol. 2010 Jul;17(7):909-15
PMID: 20601959
-
PIK3R1 mutations cause syndromic insulin resistance with lipoatrophy.
Am J Hum Genet. 2013 Jul 11;93(1):141-9
PMID: 23810378
-
Functional consequences of developmentally regulated alternative splicing.
Nat Rev Genet. 2011 Sep 16;12(10):715-29
PMID: 21921927
-
Using whole-exome sequencing to identify inherited causes of autism.
Neuron. 2013 Jan 23;77(2):259-73
PMID: 23352163
-
The genomic binding sites of a noncoding RNA.
Proc Natl Acad Sci U S A. 2011 Dec 20;108(51):20497-502
PMID: 22143764
-
Genomic dark matter: the reliability of short read mapping illustrated by the genome mappability score.
Bioinformatics. 2012 Aug 15;28(16):2097-105
PMID: 22668792
-
High-resolution mapping and characterization of open chromatin across the genome.
Cell. 2008 Jan 25;132(2):311-22
PMID: 18243105