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tardis Toolkit for Automated and Rapid DIscovery of Structural variants Requirements zlib (http://www.zlib.net)mrfast (https://github.com/BilkentCompGen/mrfast)htslib (included as submodule; http://htslib.org/)Fetching tardis git clone...

Method journals also published bioinformatics research papers http://www.sciencedirect.com/science/journal/10462023

The NovelSeq framework is designed to detect novel sequence insertions using high throughput paired-end whole genome sequencing data. http://novelseq.sourceforge.net/Home Paper at https://www.ncbi.nlm.nih.gov/pubmed/20385726

Convert masked genome to N letters. $ perl -pe '/^[^>]/ and $_=~ s/[a-z]/N/g' genomic.fna > genomic.N-masked.fna #Genome #Masked #N #Convert

Unmasking the lower case values in genome. $ perl -pe '/^[^>]/ and $_=uc' genomic.fna > genomic.unmasked.fna #Genome #Unmask #Perl #Oneliner

Update CPAN $ cpan> install CPAN; reload cpan #cpan #perl

Bedtools wiki https://code.google.com/archive/p/bedtools/wikis/Usage.wiki #Wiki #Bedtools

GraphMap - A highly sensitive and accurate mapper for long, error-prone reads http://www.nature.com/ncomms/2016/160415/ncomms11307/full/ncomms11307.htmlFeatures    Mapping position agnostic to alignment parameters.   ...

Handling #CSV file with #Perl http://perlmeme.org/tutorials/parsing_csv.html

Following are the list of Springer bioinformatics journals https://link.springer.com/search?query=bioinformatics&facet-content-type=%22Journal%22

UGC, GOI approved website for jobs in India http://www.ugc.ac.in/jobportal/

#Evolution of #Translational #Bioinformatics https://bmcmedgenomics.biomedcentral.com/articles/10.1186/s12920-017-0262-5

You can try PyInstallerm (http://www.pyinstaller.org/). It is a program that freezes (packages) Python programs into stand-alone executables, under Windows, Linux, Mac OS X, FreeBSD, Solaris and AIX. Its main advantages over similar tools are that...