Rahul Agarwal
I'm a Bioinformatician and Programmer
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Genome Browsers
Last updated 4585 days ago by Rahul Agarwal Comments (2)Genome Browser is the platform/database used for searching and retreiving sequences and annotation of genomes belong to various eukaryotes, prokaryotes, etc. Following are the weblink for different available...
Is reference genome necessary for gene expression study in transcriptome sequencing or for variant discovery in genome sequencing?
Rahul Agarwal 4615 days agoRa assembler - a de novo DNA assembler for third generation sequencing data
By biogeek 2991 days agogithub.com - Integration of the Ra assembler - a de novo DNA assembler for third generation sequencing data developed on Faculty of Electrical Engineering and Computing (FER), Ruder Boskovic Institute (RBI) and Genome Institute of Singapore (GIS). Ra is in...DeepVariant : an analysis pipeline that uses a deep neural network to call genetic variants from...
By Jit 2232 days agogithub.com - DeepVariant is an analysis pipeline that uses a deep neural network to call genetic variants from next-generation DNA sequencing data. DeepVariant is an analysis pipeline that uses a deep neural network to call genetic variants from next-generation...-
Genetic Test in India
Last updated 4590 days ago by Rahul Agarwal1.Xcode Life Sciences Pvt. Ltd.6B, Eldorado, 112, Nungambakkam High Road,Nungambakkam, Chennai 600034Tamil Nadu, India 2.Mapmygenome™Royal Demeure,HUDA Techno Enclave,Plot No. 12/2, Sector-1 500 081 Madhapur,HyderabadAP,... 320000 viruses in mammals yet to sequenced in future!!!
By Rahul Agarwal 4567 days ago70 per cent of emerging viral diseases such as HIV/AIDS, West Nile, Ebola, SARS, and influenza, are zoonoses - infections of animals that cross into humans.Tigers genome sequenced
By Rahul Agarwal 4553 days agoOnly 4.4 percent DNA difference between Tiger and house catsBFC: a standalone high-performance tool for correcting sequencing errors from Illumina sequencing...
By Jit 2836 days agogithub.com - BFC is a standalone high-performance tool for correcting sequencing errors from Illumina sequencing data. It is specifically designed for high-coverage whole-genome human data, though also performs well for small genomes. The BFC algorithm is a...DnaSP: DNA Sequence Polymorphism, is a software package for the analysis of DNA polymorphisms
By Neel 1927 days agohttp://www.ub.edu/dnasp/ - DnaSP, DNA Sequence Polymorphism, is a software package for the analysis of DNA polymorphisms using data from a single locus (a multiple sequence aligned -MSA data), or from several loci (a Multiple-MSA data, such as formats generated by some...
