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1.
2641 Accesses
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Readjoiner: a fast and memory efficient string graph-based
sequence assembler
Giorgio Gonnella, Stefan Kurtz BMC Bioinformatics 2012, 13:82 (6 May 2012)
Abstract | Provisional PDF
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2.
2504 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)
Abstract | Full text | PDF | PubMed | Cited on BioMed Central
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3.
2434 Accesses
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Tavaxy: Integrating Taverna and Galaxy workflows with cloud computing support
Mohamed Abouelhoda, Shadi A Issa, Moustafa Ghanem BMC Bioinformatics 2012, 13:77 (4 May 2012)
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4.
2336 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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5.
2101 Accesses
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A comparative evaluation of sequence classification programs
Adam L Bazinet, Michael P Cummings BMC Bioinformatics 2012, 13:92 (10 May 2012)
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6.
2096 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 Nelson BMC Bioinformatics 2012, 13:42 (19 March 2012)
Abstract | Provisional PDF
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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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7.
1630 Accesses
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Inferring high-confidence human protein-protein interactions
Xueping Yu, Anders Wallqvist, Jaques Reifman BMC Bioinformatics 2012, 13:79 (4 May 2012)
Abstract | Provisional PDF
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Editor’s summary
A novel unsupervised statistical approach for ranking protein-protein interactions called interaction detection based on shuffling reduces inherent experiment-dependent noise and increases the likelihood of detecting high confidence protein interactions.
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8.
1440 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)
Abstract | Full text | PDF | PubMed | Cited on BioMed Central
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9.
1372 Accesses
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PHYLOViZ: Phylogenetic Inference and Data Visualization
for Sequence Based Typing Methods
Alexandre P Francisco, Cátia Vaz, Pedro T Monteiro, José Melo-Cristino, Mário Ramirez, João André Carriço BMC Bioinformatics 2012, 13:87 (8 May 2012)
Abstract | Provisional PDF
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Editor’s summary
Phyloviz is an exciting free software for visualizing genotype datasets, isolating populations for epidemiological analysis, vizualising potential evolutionary relationships between bacteria and providing access to publicly available data plus potential to export high resolution images.
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10.
1304 Accesses
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Extracting semantically enriched events from
biomedical literature
Makoto Miwa, Paul Thompson, John McNaught, Douglas B Kell, Sophia Ananiadou BMC Bioinformatics 2012, 13:108 (23 May 2012)
Abstract | Provisional PDF
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11.
1299 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)
Abstract | Full text | PDF | PubMed
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12.
1259 Accesses
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Protein-RNA interface residue prediction using
machine learning: an assessment of the state of
the art
Rasna R Walia, Cornelia Caragea, Benjamin A Lewis, Fadi G Towfic, Michael Terribilini, Yasser El-Manzalawy, Drena Dobbs, Vasant Honavar BMC Bioinformatics 2012, 13:89 (10 May 2012)
Abstract | Provisional PDF
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13.
1238 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)
Abstract | Full text | PDF | PubMed | Cited on BioMed Central
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14.
1205 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)
Abstract | Provisional PDF
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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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15.
1166 Accesses
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SparSNP: Fast and memory-efficient analysis of all SNPs for phenotype prediction
Gad Abraham, Adam Kowalczyk, Justin Zobel, Michael Inouye BMC Bioinformatics 2012, 13:88 (10 May 2012)
Abstract | Provisional PDF
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16.
1097 Accesses
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MetaMapp: mapping and visualizing metabolomic
data by integrating information from biochemical
pathways and chemical and mass spectral similarity
Dinesh K Barupal, Pradeep K Haldiya, Gert Wohlgemuth, Tobias Kind, Shanker L Kothari, Kent E Pinkerton, Oliver Fiehn BMC Bioinformatics 2012, 13:99 (16 May 2012)
Abstract | Provisional PDF
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17.
1081 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)
Abstract | Provisional PDF
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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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18.
1052 Accesses
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Integrating biological knowledge into variable selection: an empirical Bayes approach with an application in cancer biology
Steven M Hill, Richard M Neve, Nora Bayani, Wen-Lin Kuo, Safiyyah Ziyad, Paul T Spellman, Joe W Gray, Sach Mukherjee BMC Bioinformatics 2012, 13:94 (11 May 2012)
Abstract | Provisional PDF
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19.
1020 Accesses
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Handling the data management needs of high-throughput sequencing data: SpeedGene, a compression algorithm for the efficient storage of genetic data
Dandi Qiao, Wai-Ki Yip, Christoph Lange BMC Bioinformatics 2012, 13:100 (16 May 2012)
Abstract | Provisional PDF
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20.
997 Accesses
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SIS: a program to generate draft genome sequence
scaffolds for prokaryotes
Zanoni Dias, Ulisses Dias, Joao C Setubal BMC Bioinformatics 2012, 13:96 (14 May 2012)
Abstract | Provisional PDF
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21.
985 Accesses
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TreeSnatcher plus: capturing phylogenetic trees
from images
Thomas Laubach, Arndt von Haeseler, Martin J. Lercher BMC Bioinformatics 2012, 13:110 (24 May 2012)
Abstract | Provisional PDF
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22.
926 Accesses
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DIPSBC - Data Integration Platform for Systems Biology Collaborations
Felix Dreher, Thomas Kreitler, Christopher Hardt, Atanas Kamburov, Reha Yildirimman, Karl Schellander, Hans Lehrach, Bodo M.H. Lange, Ralf Herwig BMC Bioinformatics 2012, 13:85 (8 May 2012)
Abstract | Provisional PDF
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23.
878 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)
Abstract | Full text | PDF | 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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24.
863 Accesses
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A unified computational model for revealing and predicting subtle subtypes of cancers
Xianwen Ren, Yong Wang, Jiguang Wang, Xiang-Sun Zhang BMC Bioinformatics 2012, 13:70 (1 May 2012)
Abstract | Provisional PDF
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25.
845 Accesses
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A Bayesian variable selection procedure to rank overlapping gene sets
Axel Skarman, Mohammad Shariati, Luc Janss, Li Jiang, Peter Sørensen BMC Bioinformatics 2012, 13:73 (3 May 2012)
Abstract | Provisional PDF
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