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1.
27396 Accesses
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Statistical analysis of real-time PCR data
Joshua S Yuan, Ann Reed, Feng Chen, C Neal Stewart BMC Bioinformatics 2006, 7:85 (22 February 2006)
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| PubMed | Cited on BioMed Central
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2.
21626 Accesses
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Cloud BioLinux: pre-configured and on-demand bioinformatics computing for the genomics community
Konstantinos Krampis, Tim Booth, Brad Chapman, Bela Tiwari, Mesude Bicak, Dawn Field, Karen E Nelson BMC Bioinformatics 2012, 13:42 (19 March 2012)
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| PubMed | Cited on BioMed Central
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Editor’s summary
Cloud BioLinux includes over 135 pre-configured bioinformatics tools for sequence alignment, clustering, assembly, display and phylogeny, aimed at reducing costs to researchers of maintaining and configuring hardware, and encouraging sharing of codebase.
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3.
17176 Accesses
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Evaluation of statistical methods for normalization and differential expression in mRNA-Seq experiments
James H Bullard, Elizabeth Purdom, Kasper D Hansen, Sandrine Dudoit BMC Bioinformatics 2010, 11:94 (18 February 2010)
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| PubMed | Cited on BioMed Central
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4.
13537 Accesses
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RSEM: accurate transcript quantification from RNA-Seq data with or without a reference genome
Bo Li, Colin N Dewey BMC Bioinformatics 2011, 12:323 (4 August 2011)
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| PubMed | Cited on BioMed Central
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Editor’s summary
RSEM is a new user-friendly software tool for quantifying transcript abundance from RNA-seq data that does not rely on a reference genome and is particularly useful for quantification with de novo transcriptome assemblies
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5.
12176 Accesses
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VennDiagram: a package for the generation of highly-customizable Venn and Euler diagrams in R
Hanbo Chen, Paul C Boutros BMC Bioinformatics 2011, 12:35 (26 January 2011)
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| PubMed | Cited on BioMed Central
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6.
11810 Accesses
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WGCNA: an R package for weighted correlation network analysis
Peter Langfelder, Steve Horvath BMC Bioinformatics 2008, 9:559 (29 December 2008)
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| PubMed | Cited on BioMed Central
| F1000 Biology
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7.
9314 Accesses
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GEOGLE: context mining tool for the correlation between gene expression and the phenotypic distinction
Yao Yu, Kang Tu, Siyuan Zheng, Yun Li, Guohui Ding, Jie Ping, Pei Hao, Yixue Li BMC Bioinformatics 2009, 10:264 (25 August 2009)
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| PubMed | Cited on BioMed Central
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8.
9203 Accesses
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Primer-BLAST: A tool to design target-specific primers for polymerase chain reaction
Jian Ye, George Coulouris, Irena Zaretskaya, Ioana Cutcutache, Steve Rozen, Thomas L Madden BMC Bioinformatics 2012, 13:134 (18 June 2012)
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| PubMed | Cited on BioMed Central
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9.
8311 Accesses
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BioWord: A sequence manipulation suite for Microsoft Word
Laura J Anzaldi, Daniel Muñoz-Fernández, Ivan Erill BMC Bioinformatics 2012, 13:124 (7 June 2012)
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10.
8182 Accesses
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An overview of the Hadoop/MapReduce/HBase framework and its current applications in bioinformatics
Ronald C Taylor BMC Bioinformatics 2010, 11(Suppl 12):S1 (21 December 2010)
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11.
8037 Accesses
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The development and validation of the Virtual Tissue Matrix, a software application that facilitates the review of tissue microarrays on line
Catherine M Conway, Deirdre O'Shea, Sallyann O'Brien, Darragh K Lawler, Graham D Dodrill, Anthony O'Grady, Helen Barrett, Christian Gulmann, Lorraine O'Driscoll, William M Gallagher, Elaine W Kay, Daniel G O'Shea BMC Bioinformatics 2006, 7:256 (17 May 2006)
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| PubMed | Cited on BioMed Central
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12.
7923 Accesses
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Mapsembler, targeted and micro assembly of large NGS datasets on a desktop computer
Pierre Peterlongo, Rayan Chikhi BMC Bioinformatics 2012, 13:48 (23 March 2012)
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Editor’s summary
Mapsembler, a sequence assembly tool for desktop computers, uses NGS reads from newly sequenced, non-assembled genomes or transcriptomes to provide targeted assemblies and has retrieved known gene fusions in human cancer and discovered new ones
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13.
7716 Accesses
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An integrative variant analysis suite for whole exome next-generation sequencing data
Danny Challis, Jin Yu, Uday S Evani, Andrew R Jackson, Sameer Paithankar, Cristian Coarfa, Aleksandar Milosavljevic, Richard A Gibbs, Fuli Yu BMC Bioinformatics 2012, 13:8 (12 January 2012)
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| PubMed | Cited on BioMed Central
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Editor’s summary
The Atlas2 is an analysis suite for variant calling in whole exome sequencing that combines regression models and user-adjustable cutoffs in order to separate true SNPs and INDELs from sequencing and mapping errors, with high sensitivity
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14.
7700 Accesses
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Statistical significance of quantitative PCR
Yann Karlen, Alan McNair, Sébastien Perseguers, Christian Mazza, Nicolas Mermod BMC Bioinformatics 2007, 8:131 (20 April 2007)
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15.
7679 Accesses
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Optimizing de novo transcriptome assembly from short-read RNA-Seq data: a comparative study
Qiong-Yi Zhao, Yi Wang, Yi-Meng Kong, Da Luo, Xuan Li, Pei Hao BMC Bioinformatics 2011, 12(Suppl 14):S2 (14 December 2011)
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| PubMed | Cited on BioMed Central
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16.
7036 Accesses
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The metagenomics RAST server – a public resource for the automatic phylogenetic and functional analysis of metagenomes
F Meyer, D Paarmann, M D'Souza, R Olson, EM Glass, M Kubal, T Paczian, A Rodriguez, R Stevens, A Wilke, J Wilkening, RA Edwards BMC Bioinformatics 2008, 9:386 (19 September 2008)
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| PubMed | Cited on BioMed Central
| F1000 Biology
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17.
6939 Accesses
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BioWarehouse: a bioinformatics database warehouse toolkit
Thomas J Lee, Yannick Pouliot, Valerie Wagner, Priyanka Gupta, David WJ Stringer-Calvert, Jessica D Tenenbaum, Peter D Karp BMC Bioinformatics 2006, 7:170 (23 March 2006)
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18.
6580 Accesses
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GC-Content Normalization for RNA-Seq Data
Davide Risso, Katja Schwartz, Gavin Sherlock, Sandrine Dudoit BMC Bioinformatics 2011, 12:480 (17 December 2011)
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Editor’s summary
The combination of three different strategies for GC-content normalization of RNA-seq data leads to more accurate estimations of gene expression levels and fold-changes, making statistical inference of differential expression less prone to false discoveries.
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19.
6567 Accesses
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Tavaxy: Integrating Taverna and Galaxy workflows with cloud computing support
Mohamed Abouelhoda, Shadi Issa, Moustafa Ghanem BMC Bioinformatics 2012, 13:77 (4 May 2012)
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| PubMed | Cited on BioMed Central
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20.
6448 Accesses
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Cancer bioinformatics: A new approach to systems clinical medicine
Duojiao Wu, Catherine M Rice, Xiangdong Wang BMC Bioinformatics 2012, 13:71 (1 May 2012)
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| PubMed | Cited on BioMed Central
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21.
6445 Accesses
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The MULTICOM toolbox for protein structure prediction
Jianlin Cheng, Jilong Li, Zheng Wang, Jesse Eickholt, Xin Deng BMC Bioinformatics 2012, 13:65 (30 April 2012)
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Editor’s summary
MULTICOM Toolbox contains an array of extensively tested and high performance tools aimed at reducing the growing gap between derived protein sequences and structural determination, that includes both secondary and tertiary structure predictors
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22.
6431 Accesses
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MPprimer: a program for reliable multiplex PCR primer design
Zhiyong Shen, Wubin Qu, Wen Wang, Yiming Lu, Yonghong Wu, Zhifeng Li, Xingyi Hang, Xiaolei Wang, Dongsheng Zhao, Chenggang Zhang BMC Bioinformatics 2010, 11:143 (18 March 2010)
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23.
6299 Accesses
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pROC: an open-source package for R and S+ to analyze and compare ROC curves
Xavier Robin, Natacha Turck, Alexandre Hainard, Natalia Tiberti, Frédérique Lisacek, Jean-Charles Sanchez, Markus Müller BMC Bioinformatics 2011, 12:77 (17 March 2011)
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| PubMed | Cited on BioMed Central
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24.
6069 Accesses
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MUSCLE: a multiple sequence alignment method with reduced time and space complexity
Robert C Edgar BMC Bioinformatics 2004, 5:113 (19 August 2004)
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| PubMed | Cited on BioMed Central
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25.
6017 Accesses
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UniFrac – An online tool for comparing microbial community diversity in a phylogenetic context
Catherine Lozupone, Micah Hamady, Rob Knight BMC Bioinformatics 2006, 7:371 (7 August 2006)
Abstract | Full text | PDF
| PubMed | Cited on BioMed Central
| F1000 Biology
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Editor’s summary
A new online open-access tool, Unifrac, provides multivariate analysis techniques for comparing microbial communities in a phylogenetic context and contributes to our understanding of many microbial interactions and processes.
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