BOL

There are a lot of universities offering Bachelor or Master degree in Pakistan. Following are the list of few intitute/universities

sepsis-omics.github.io - This is a tutorial for a workshop on long-read (PacBio) genome assembly. It demonstrates how to use long PacBio sequencing reads to assemble a bacterial genome, and includes additional steps for circularising, trimming, finding plasmids, and...

Research Associate (RA) under Network Project on Agricultural Bioinformatics Name of the Project : Network Project on Agricultural Bioinformatics Number of positions One Qualifications : Ph.D Degree in Bioinformatics/Biotechnology/...

github.com - Flye is a de novo assembler for single molecule sequencing reads, such as those produced by PacBio and Oxford Nanopore Technologies. It is designed for a wide range of datasets, from small bacterial projects to large mammalian-scale assemblies. The...

Walk-in-interview will be held on 23 February, 2015 at 11.00 a.m. for the following temporary positions in the DBT (U-EXCEL) sponsored project entitled “Sequencing genomes of some bacteria that invade/resides in tomato plant” under the Principal...

github.com - MitoZ is a Python3-based toolkit which aims to automatically filter pair-end raw data (fastq files), assemble genome, search for mitogenome sequences from the genome assembly result, annotate mitogenome (genbank file as result), and mitogenome...

No. ACTREC/Advt./ 7 /2015 Title of the Project Research Associate (One position) DBTs Biotechnology/Bioinformatics training centre PI Dr. Ashok Varma Duration of the Project Six Months from the date of appointment, can be extended...

github.com - A program to detect recombination hotspots using population genetic data. More at https://github.com/auton1/LDhot

Be proficient in LINUX, know perl or python, understand biology and Next Generation Sequencing. The intern will port Agile Assay Design pipelines into Galaxy. The intern will also learn to develope his/her own bioinformatics pipelines for PCR or...

BBSplit internally uses BBMap to map reads to multiple genomes at once, and determine which genome they match best. This is different than with ordinary mapping. If a genome (say, human) contains an exact repeat somewhere, reads mapping to it will...