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1.
34576 Accesses
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Differential expression analysis for sequence count data
Simon Anders, Wolfgang Huber Genome Biology 2010, 11:R106 (27 October 2010)
Abstract | Full text | PDF
| PubMed | Cited on BioMed Central |
| F1000 Biology
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Editor’s summary
DEseq allows the determination of differential expression of read count data from RNA-seq or ChIP-seq experiments
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2.
31177 Accesses
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Ultrafast and memory-efficient alignment of short DNA sequences to the human genome
Ben Langmead, Cole Trapnell, Mihai Pop, Steven L Salzberg Genome Biology 2009, 10:R25 (4 March 2009)
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| PubMed | Cited on BioMed Central
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Editor’s summary
Bowtie: a new ultrafast memory-efficient tool for the alignment of short DNA sequence reads to large genomes.
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3.
27870 Accesses
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Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes
Jo Vandesompele, Katleen De Preter, Filip Pattyn, Bruce Poppe, Nadine Van Roy, Anne De Paepe, Frank Speleman Genome Biology 2002, 3:research0034-research0034.11 (18 June 2002)
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| PubMed | Cited on BioMed Central |
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Editor’s summary
Using real-time reverse transcription PCR ten housekeeping genes from different abundance and functional classes in various human tissues were evaluated. The conventional use of a single gene for normalization leads to relatively large errors in a significant proportion of samples tested.
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4.
27852 Accesses
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VlincRNAs controlled by retroviral elements are a hallmark of pluripotency and cancer
Georges St Laurent, Dmitry Shtokalo, Biao Dong, Michael R Tackett, Xiaoxuan Fan, Sandra Lazorthes, Estelle Nicolas, Nianli Sang, Timothy J Triche, Timothy A McCaffrey, Weidong Xiao, Philipp Kapranov Genome Biology 2013, 14:R73 (22 July 2013)
Abstract | Provisional PDF
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Editor’s summary
The expression of vlincRNAs from retroviral promoters is correlated with pluripotency and malignancy
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5.
26880 Accesses
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Functional analysis of transcription factor binding sites in human promoters
Troy W Whitfield, Jie Wang, Patrick J Collins, E Christopher Partridge, Shelley Aldred, Nathan D Trinklein, Richard M Myers, Zhiping Weng Genome Biology 2012, 13:R50 (5 September 2012)
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| PubMed | Cited on BioMed Central
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Editor’s summary
TFBSs are predicted from ENCODE data, and experiments in four cell lines find 70% to be functional
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6.
23101 Accesses
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Classification of human genomic regions based on experimentally determined binding sites of more than 100 transcription-related factors
Kevin Y Yip, Chao Cheng, Nitin Bhardwaj, James B Brown, Jing Leng, Anshul Kundaje, Joel Rozowsky, Ewan Birney, Peter Bickel, Michael Snyder, Mark Gerstein Genome Biology 2012, 13:R48 (5 September 2012)
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| PubMed | Cited on BioMed Central
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Editor’s summary
Machine learning analysis of ENCODE data for 100 transcription factors reveals six classes of genomic regions
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7.
22137 Accesses
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Modeling gene expression using chromatin features in various cellular contexts
Xianjun Dong, Melissa C Greven, Anshul Kundaje, Sarah Djebali, James B Brown, Chao Cheng, Thomas R Gingeras, Mark Gerstein, Roderic Guigó, Ewan Birney, Zhiping Weng Genome Biology 2012, 13:R53 (5 September 2012)
Abstract | Full text | PDF
| PubMed | Cited on BioMed Central
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Editor’s summary
Models for linking gene expression with chromatin features vary according to cellular context and RNA measurement method
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8.
20644 Accesses
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From RNA-seq reads to differential expression results
Alicia Oshlack, Mark D Robinson, Matthew D Young Genome Biology 2010, 11:220 (22 December 2010)
Abstract | Full text | PDF
| PubMed | Cited on BioMed Central
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Editor’s summary
Many methods and tools are available for preprocessing high-throughput RNA sequencing data and detecting differential expression.
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9.
20110 Accesses
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A 10-step guide to party conversation for bioinformaticians
Alicia Oshlack Genome Biology 2013, 14:104 (29 January 2013)
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Editor’s summary
Alicia Oshlack's 10-step guide to party conversation for bioinformaticians
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10.
19939 Accesses
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The GENCODE pseudogene resource
Baikang Pei, Cristina Sisu, Adam Frankish, Cédric Howald, Lukas Habegger, Xinmeng Mu, Rachel Harte, Suganthi Balasubramanian, Andrea Tanzer, Mark Diekhans, Alexandre Reymond, Tim J Hubbard, Jennifer Harrow, Mark B Gerstein Genome Biology 2012, 13:R51 (5 September 2012)
Abstract | Full text | PDF
| PubMed | Cited on BioMed Central
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Editor’s summary
The GENCODE pseudogene resource includes evidence for dead genes undergoing resurrection
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11.
19299 Accesses
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Analysis of variation at transcription factor binding sites in Drosophila and humans
Mikhail Spivakov, Junaid Akhtar, Pouya Kheradpour, Kathryn Beal, Charles Girardot, Gautier Koscielny, Javier Herrero, Manolis Kellis, Eileen EM Furlong, Ewan Birney Genome Biology 2012, 13:R49 (5 September 2012)
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| PubMed | Cited on BioMed Central
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Editor’s summary
Transcription factor binding site variability in fly and human provides evidence for a buffering phenomenon
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12.
18243 Accesses
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A scaling normalization method for differential expression analysis of RNA-seq data
Mark D Robinson, Alicia Oshlack Genome Biology 2010, 11:R25 (2 March 2010)
Abstract | Full text | PDF
| PubMed | Cited on BioMed Central
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Editor’s summary
A novel and empirical method for normalization of RNA-seq data is presented
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13.
18183 Accesses
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EMIRGE: reconstruction of full-length ribosomal genes from microbial community short read sequencing data
Christopher S Miller, Brett J Baker, Brian C Thomas, Steven W Singer, Jillian F Banfield Genome Biology 2011, 12:R44 (19 May 2011)
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Editor’s summary
Reconstructing full length rRNA sequences from short reads to estimate microbial community structure
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14.
16367 Accesses
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TopHat2: accurate alignment of transcriptomes in the presence of insertions, deletions and gene fusions
Daehwan Kim, Geo Pertea, Cole Trapnell, Harold Pimentel, Ryan Kelley, Steven L Salzberg Genome Biology 2013, 14:R36 (25 April 2013)
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Editor’s summary
A major update to TopHat, the popular Bowtie-based spliced aligner
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15.
15567 Accesses
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The western painted turtle genome, a model for the evolution of extreme physiological adaptations in a slowly evolving lineage
H Bradley Shaffer, Patrick Minx, Daniel E Warren, Andrew M Shedlock, Robert C Thomson, Nicole Valenzuela, John Abramyan, Chris T Amemiya, Daleen Badenhorst, Kyle K Biggar, Glen M Borchert, Christopher W Botka, Rachel M Bowden, Edward L Braun, Anne M Bronikowski, Benoit G Bruneau, Leslie T Buck, Blanche Capel, Todd A Castoe, Mike Czerwinski, Kim D Delehaunty, Scott V Edwards, Catrina C Fronick, Matthew K Fujita, Lucinda Fulton, Tina A Graves, Richard E Green, Wilfried Haerty, Ramkumar Hariharan, Omar Hernandez et al.
Genome Biology 2013, 14:R28 (28 March 2013)
Abstract | Full text | PDF
| PubMed | Cited on BioMed Central
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Editor’s summary
The genome of the western painted turtle, Chrysemys picta bellii, reveals insights into its extreme tolerance to anoxia and freezing
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16.
15508 Accesses
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The draft genome and transcriptome of Cannabis sativa
Harm van Bakel, Jake M Stout, Atina G Cote, Carling M Tallon, Andrew G Sharpe, Timothy R Hughes, Jonathan E Page Genome Biology 2011, 12:R102 (20 October 2011)
Abstract | Full text | PDF
| PubMed | Cited on BioMed Central |
| F1000 Biology
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Editor’s summary
The genome and transcriptome of marijuana, and comparative analysis with resequenced hemp, explains the genetic basis of psychoactivity
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17.
14068 Accesses
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Quartz-Seq: a highly reproducible and sensitive single-cell RNA sequencing method, reveals non-genetic gene-expression heterogeneity
Yohei Sasagawa, Itoshi Nikaido, Tetsutaro Hayashi, Hiroki Danno, Kenichiro D Uno, Takeshi Imai, Hiroki R Ueda Genome Biology 2013, 14:R31 (17 April 2013)
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Editor’s summary
Quartz-Seq is a method for performing single cell RNA-seq which displays high reproducibility
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18.
14038 Accesses
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Model-based Analysis of ChIP-Seq (MACS)
Yong Zhang, Tao Liu, Clifford A Meyer, Jérôme Eeckhoute, David S Johnson, Bradley E Bernstein, Chad Nusbaum, Richard M Myers, Myles Brown, Wei Li, X Shirley Liu Genome Biology 2008, 9:R137 (17 September 2008)
Abstract | Full text | PDF
| PubMed | Cited on BioMed Central
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Editor’s summary
MACS performs model-based analysis of ChIP-Seq data generated by short read sequencers.
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19.
13808 Accesses
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The Transcription Factor Encyclopedia
Dimas Yusuf, Stefanie L Butland, Magdalena I Swanson, Eugene Bolotin, Amy Ticoll, Warren A Cheung, Xiao Cindy Zhang, Christopher TD Dickman, Debra L Fulton, Jonathan S Lim, Jake M Schnabl, Oscar HP Ramos, Mireille Vasseur-Cognet, Charles N de Leeuw, Elizabeth M Simpson, Gerhart U Ryffel, Eric W-F Lam, Ralf Kist, Miranda SC Wilson, Raquel Marco-Ferreres, Jan J Brosens, Leonardo L Beccari, Paola Bovolenta, Bérénice A Benayoun, Lara J Monteiro, Helma DC Schwenen, Lars Grontved, Elizabeth Wederell, Susanne Mandrup, Reiner A Veitia et al.
Genome Biology 2012, 13:R24 (29 March 2012)
Abstract | Full text | PDF
| PubMed | Cited on BioMed Central |
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Editor’s summary
A high quality compendium of transcription factor data that allows researchers to add new data via a peer-review system
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20.
13510 Accesses
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Improving RNA-Seq expression estimates by correcting for fragment bias
Adam Roberts, Cole Trapnell, Julie Donaghey, John L Rinn, Lior Pachter Genome Biology 2011, 12:R22 (16 March 2011)
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| PubMed | Cited on BioMed Central
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Editor’s summary
An extension to Cufflinks corrects bias in RNA-seq datasets
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21.
13494 Accesses
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Analyzing and minimizing PCR amplification bias in Illumina sequencing libraries
Daniel Aird, Michael G Ross, Wei-Sheng Chen, Maxwell Danielsson, Timothy Fennell, Carsten Russ, David B Jaffe, Chad Nusbaum, Andreas Gnirke Genome Biology 2011, 12:R18 (21 February 2011)
Abstract | Full text | PDF
| PubMed | Cited on BioMed Central
| F1000 Biology
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Editor’s summary
The optimization of PCR amplification steps in Illumina libraries significantly reduces sequencing bias
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22.
13291 Accesses
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Bioconductor: open software development for computational biology and bioinformatics
Robert C Gentleman, Vincent J Carey, Douglas M Bates, Ben Bolstad, Marcel Dettling, Sandrine Dudoit, Byron Ellis, Laurent Gautier, Yongchao Ge, Jeff Gentry, Kurt Hornik, Torsten Hothorn, Wolfgang Huber, Stefano Iacus, Rafael Irizarry, Friedrich Leisch, Cheng Li, Martin Maechler, Anthony J Rossini, Gunther Sawitzki, Colin Smith, Gordon Smyth, Luke Tierney, Jean YH Yang, Jianhua Zhang Genome Biology 2004, 5:R80 (15 September 2004)
Abstract | Full text | PDF
| PubMed | Cited on BioMed Central
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Editor’s summary
A detailed description of the aims and methods of the Bioconductor project, an initiative for the collaborative creation of extensible software for computational biology and bioinformatics.
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23.
13143 Accesses
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Cell type-specific binding patterns reveal that TCF7L2 can be tethered to the genome by association with GATA3
Seth Frietze, Rui Wang, Lijing Yao, Yu Tak, Zhenqing Ye, Malaina Gaddis, Heather Witt, Peggy J Farnham, Victor X Jin Genome Biology 2012, 13:R52 (5 September 2012)
Abstract | Full text | PDF
| PubMed
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Editor’s summary
The transcription factor TCF7L2 can be tethered to the genome by GATA3, and therefore can target sites lacking its own motif
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24.
13027 Accesses
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CellProfiler: image analysis software for identifying and quantifying cell phenotypes
Anne E Carpenter, Thouis R Jones, Michael R Lamprecht, Colin Clarke, In Kang, Ola Friman, David A Guertin, Joo Chang, Robert A Lindquist, Jason Moffat, Polina Golland, David M Sabatini Genome Biology 2006, 7:R100 (31 October 2006)
Abstract | Full text | PDF
| PubMed | Cited on BioMed Central
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Editor’s summary
CellProfiler, the first free, open-source system for flexible and high-throughput cell image analysis is described.
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25.
12913 Accesses
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An encyclopedia of mouse DNA elements (Mouse ENCODE)
Mouse ENCODE Consortium, John A Stamatoyannopoulos, Michael Snyder, Ross Hardison, Bing Ren, Thomas Gingeras, David M Gilbert, Mark Groudine, Michael Bender, Rajinder Kaul, Theresa Canfield, Erica Giste, Audra Johnson, Mia Zhang, Gayathri Balasundaram, Rachel Byron, Vaughan Roach, Peter J Sabo, Richard Sandstrom, A Sandra Stehling, Robert E Thurman, Sherman M Weissman, Philip Cayting, Manoj Hariharan, Jin Lian, Yong Cheng, Stephen G Landt, Zhihai Ma, Barbara J Wold, Job Dekker et al.
Genome Biology 2012, 13:418 (13 August 2012)
Abstract | Full text | PDF
| PubMed | Cited on BioMed Central
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Editor’s summary
The Mouse ENCODE Consortium is applying the same experimental pipelines developed for human ENCODE to annotate the mouse genome
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