Comment on "Coronavirus Resources !"
Some important resources here https://artic.network/ncov-20191036 days ago
Comment on "Calling variants in non-diploid systems"
FreeBayes is widely used for calling variants in diploid systems. However, it can also be used for calling variants in pooled samples where the number of samples is not known. This... --pooled-continuous option of FreeBayes to generate frequency-...1036 days ago
1094 days ago
Comment on "Important Journals, Blogs and Forums for Bioinformaticians"
Bioinformatics Journals Ranks from Google Scholar 1: Bioinformatics Journals (the most rece...nbsp;(9.617 :: 7.017) Bioinformatics (4.981 :: 8.136)....465) Algorithms for Molecular Biology (1.463 :: 2.155)...etics (4.780 :: 5.081) Frontiers in Genetics G3-Genes...1097 days ago
Comment on "Modular, efficient and constant-memory single-cell RNA-seq preprocessing"
scRNA-seq_intro https://pachterlab.github.io/kallistobustools/tutorials/scRNA-seq_intro/python/scRNA-seq_intro/1118 days ago
Comment on "List of non-commercial NGS genotype-calling software"
Delly – Structural variant discovery by integrated paired-end and split-read analysis. [ paper-2012 ] lumpy – lum...tural variant discovery. [ paper-2014 ] manta &ndas...fication Software Suite. [ paper-2017 ]smoove &ndash...1135 days ago
Comment on "Bioinformatics Companies in India"
Bioinformatics startup https://www.genique.co/1135 days ago
1139 days ago
Comment on "How to install Perl modules manually, using CPAN command, and other quick ways"
# envname is the name of your (existing) conda env conda activate envname # cpanm is available on either conda-forge or # bioconda, so add conda-forge (or look up # how to set u...a-forge # Install cpanm conda install perl-app-cpanminus # packagename...1174 days ago
Comment on "chromoMap-An R package for Interactive visualization and mapping of human chromosomes"
Detail documentation is available at https://lakshay-anand.github.io/chromoMap/docs.html1197 days ago