Central University of South Bihar
(Established under Central Universities Act, 2009)
BIT Campus, PO: B.V. College,
Patna – 800 014 (Bihar)
Employment Notice No. CUSB / 27 / Faculty / 2015
Appointment for Faculty Positions Applications...
japsa.readthedocs.io - npScarf (jsa.np.npscarf) is a program that connect contigs from a draft genomes to generate sequences that are closer to finish. These pipelines can run on a single laptop for microbial datasets. In real-time mode, it can be integrated with simple...
Rajiv Gandhi Centre for Biotechnology (RGCB), Thiruvananthapuram
Job Code: 060815(10)Y
Jr Research Fellow Posts At Rajiv Gandhi Centre for Biotechnology
Rajiv Gandhi Centre for Biotechnology (RGCB) invites applications to recruit on vacant...
bitbucket.org - SimLoRD is a read simulator for third generation sequencing reads and is currently focused on the Pacific Biosciences SMRT error model.
Reads are simulated from both strands of a provided or randomly generated reference sequence.
The reference...
DEPARTMENT OF BIOTECHNOLOGY
ALL INDIA INSTITUTE OF MEDICAL SCIENCES
NEW DELHI-110029
Requirement of Senior Research Fellow Applications are invited for the following vacancy under Research project entitled “Exploiting temporal transcription...
github.com - Development packages for zlib and libbz2 are needed, as well as a standard compiler environment. On Ubuntu, this can be installed via:
sudo apt-get install build-essential libtool automake zlib1g-dev libbz2-dev pkg-config
On MacOS, the Apple...
This 2 day symposium will focus on topics in the below mentioned areas.
Experts from India and Japan in this fields will deliver lectures and contribute in discussions. This will provide an opportunity to the participants to interact and...
github.com - Wtdbg2 is a de novo sequence assembler for long noisy reads produced by PacBio or Oxford Nanopore Technologies (ONT). It assembles raw reads without error correction and then builds the consensus from intermediate assembly...
bioinfo.ut.ee - FastGT is a program package for whole-genome genotyping of genome variants directly from raw sequencing reads. It is written in C and runs in Linux. FastGT uses a list of variant-specific k-mer pairs that are unique in human genome, counts the...