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ORCIDSource Code for Biology and Medicine, Volume 11
Volume 11, Number 1, December 2016
- Jitsuki Sawamura, Shigeru Morishita, Jun Ishigooka:
Symmetrical treatment of "Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition", for major depressive disorders. 1 - Vasanth R. Singan
, Jeremy C. Simpson:
Implementation of the Rank-Weighted Co-localization (RWC) algorithm in multiple image analysis platforms for quantitative analysis of microscopy images. 2 - Refat Sharmin, Abul Bashar Mir Md Khademul Islam:
Conserved antigenic sites between MERS-CoV and Bat-coronavirus are revealed through sequence analysis. 3 - Samson S. Kiware, Tanya L. Russell, Zacharia John Mtema, Alpha D. Malishee, Prosper Chaki, Dickson Lwetoijera, Javan Chanda, Dingani Chinula, Silas Majambere, John E. Gimnig, Thomas A. Smith, Gerry F. Killeen:
A generic schema and data collection forms applicable to diverse entomological studies of mosquitoes. 4 - Fuquan Zhang:
A flexible tool to plot a genomic map for single nucleotide polymorphisms. 5 - Deena M. A. Gendoo, Benjamin Haibe-Kains:
MM2S: personalized diagnosis of medulloblastoma patients and model systems. 6 - Ana Gabriella de Oliveira Sardinha, Ceres Nunes de Resende Oyama, Armando de Mendonça Maroja, Ivan F. Costa:
Implementation and clinical application of a deformation method for fast simulation of biological tissue formed by fibers and fluid. 7 - Caleb F. Davis, Deborah I. Ritter, David A. Wheeler, Hongmei Wang, Yan Ding, Shannon P. Dugan, Matthew N. Bainbridge, Donna M. Muzny, Pulivarthi H. Rao, Tsz-Kwong Man, Sharon E. Plon, Richard A. Gibbs, Ching C. Lau:
SV-STAT accurately detects structural variation via alignment to reference-based assemblies. 8 - John M. Macdonald, Paul C. Boutros:
Log: : ProgramInfo: A Perl module to collect and log data for bioinformatics pipelines. 9 - Brigitte Glanzmann, Hendri Herbst, Craig J. Kinnear, Marlo Möller, Junaid Gamieldien, Soraya Bardien:
A new tool for prioritization of sequence variants from whole exome sequencing data. 10 - Lindsay V. Clark, Erik J. Sacks:
TagDigger: user-friendly extraction of read counts from GBS and RAD-seq data. 11 - Toshiki Takeuchi, Atsuo Yamada, Takashi Aoki, Kunihiro Nishimura:
cljam: a library for handling DNA sequence alignment/map (SAM) with parallel processing. 12 - Markus Riester, Angad P. Singh, Angela Rose Brannon, Kun Yu, Catarina D. Campbell, Derek Y. Chiang, Michael P. Morrissey:
PureCN: copy number calling and SNV classification using targeted short read sequencing. 13 - Syed Haider, Daryl Waggott, Emilie Lalonde, Clement Fung, Fei-Fei Liu, Paul C. Boutros:
A bedr way of genomic interval processing. 14
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