github.com - With advances in Cancer Genomics, Mutation Annotation Format (MAF) is being widely accepted and used to store somatic variants detected. The Cancer Genome Atlas Project has sequenced over 30 different cancers with sample size of each cancer type...
SCHOOL OF CHEMISTRY, UNIVERSITY OF HYDERABAD
Applications on plain paper along with details of CV (relevant photocopies of their
qualifications/experience and reprints of published work to be attached) are invited from qualified candidates for...
github.com - chromeister: An ultra fast, heuristic approach to detect conserved signals in extremely large pairwise genome comparisons.
USAGE:
-query: sequence A in fasta format
-db: sequence B in fasta format
-out: output matrix
-kmer Integer: k>1...
Ref: 13/102900
Available immediately until 30th November 2015, to work on the development of bioinformatics approaches to aid analysis of data derived from the metabolomic profiling of biological matrices. The successful applicant will lead...
www.science.org - The completed regions include all centromeric satellite arrays, recent segmental duplications, and the short arms of all five acrocentric chromosomes, unlocking these complex regions of the genome to variational and functional studies.
NATIONAL JALMA INSTITUTE OF LEPROSY AND OTHER MYCOBACTERIAL DISEASES
(INDIAN COUNCIL OF MEDICAL RESEARCH)
P.O BOX 101,
Dr. M. Miyazaki Marg,
Tajganj, Agra - 282001
Applications are invited for a walk-in interview to be held in the Seminar...
github.com - igvjs - a create-react-app with igv package from npm installed. the igv.js is instrumented to output "DONE" to the console when finished, and to have an increased fetchSizeLimit (which is otherwise git in CRAM longread tests)
jb2-web - stock...
Gagneur lab at Gene Center, Ludwig-Maximilians-Universitaet, Munich, Germany
Deadline for applications : January 15, 2014.
Description :
We seek a talented and motivated post-doc to develop computational methods for inferring the molecular...
Like in case of plant genomes where nature of genome is too complex and huge in size to accomplish complete de novo assembly by current sequencing technology. What would be alternate solution? Can we live in reference free world?
Only bioinformatician can understand that multiplication and division are different but same thing :)
Disclaimer: This cartoon is solely designed to create humour and fun, not to offend any computer experts.