Results for "In-depth"
Blogs
How to Prepare your Bioinformatics CV ?
Preparing a CV is also an art as well as a requirement for a person applying for a job . Curriculum Vitae is the first impression on the employer so it should be the bes...3553 days ago
Structural variation: the hidden genomic treasure
Genome re-sequencing projects have revealed substantial amounts of genetic variation between individuals extending beyond single nucleotide polymorphisms (SNPs) and shor...2882 days ago
- +3 more Blogs
Bookmarks
- HiCdat: a fast and easy-to-use Hi-C data analysis tool HiCdat is easy-to-use and provides solutions starting from aligned reads up to in-depth analyses. Importantly, HiCdat is focusse...
3185 days ago
CovCal: Coverage / Read Count Calculator
Coverage / Read Count Calculator Calculate how much sequencing you need to hit a target depth of coverage (or vice versa). Instructions: set the read length/configurat...2345 days ago
- +19 more Bookmarks
Pages
Genome Assembly Tools and Software - PART2 !!
The genome assemblers generally take a file of short sequence reads and a file of quality-value as the input. Since the quality-value file for the high throughput short...2865 days ago
Awesome perl frameworks, libraries and software - PART 4
...min. Alpha. SethRobertson/git-what-branch - Discover what branch a commit is on, or how it got to a named branch shabble/irssi-docs - In-depth documentation of the Irssi IR...2674 days ago
Top-level pages
List of In-silico Binding Site Prediction Tools
Following are the list of In-silico Binding Site Prediction in Proteins tools CASTp : http://sts.bioengr.uic.edu/castp/ Computed Atlas of Surface Topography of pr...3923 days ago
Commercial and public next-gen-seq (NGS) software
Integrated solutions CLCbio Genomics Workbench - de novo and reference assembly of Sanger, Roche FLX, Illumina, Helicos, and SOLiD data. Commercial next-gen-seq software...3698 days ago
- +10 more Top-level pages
Wire posts
Opportunity posts
Postodoc in Computational/Systems Biology and Machine Learning
...disorders. You have a PhD in Computational Science, Bioinformatics, or equivalent. Especially relevant skills for the profile are: 1. In-depth understanding and implementat...3858 days ago
Opening for RA/extended SRF in Bioinformatics project by DBT at Bose Institute
...m (IGCS) for Biomolecular Modeling, Molecular Dynamics & Structures” Desired Profile : Ph.D degree in Biological or Chemical Sciences with in-depth understanding of protein stru...3533 days ago
- +6 more Opportunity posts
ResearchLabs posts
- The laboratory is focused on the discovery and analysis of structural variation (SVs) from genomic sequence data. As part of the 1000 Genomes Project and other endeavors...
3172 days ago
Video
How to sequence the human genome - Mark J. Kiel
...tists are now able to know the sequence of letters that makes up an individual genome relatively quickly and inexpensively. Mark J. Kiel takes an in-depth look at the science behind th...3807 days ago
Bio-Scripts
- # get total number of bases covered at MIN_COVERAGE_DEPTH or higher samtools mpileup mapping_result_sorted.bam | awk -v X="${MIN_COVERAGE_DEPTH}" '$4>=X' | wc -l 32876...
2389 days ago
- jitendra@jitendra-UNLOCK-INSTALL[SNP] wget https://github.com/broadinstitute/gatk/releases/download/4.0.2.1/gatk-4.0.2.1.zip --2018-08-30 11:47:20-- https://github.com...
2255 days ago
- +6 more Bio-Scripts
Comments
- AfterQC AfterQC - Automatic Filtering, Trimming, Error Removing and Quality Control for fastq data. dupRadar dupRadar. An R package which provides...
2317 days ago
Comment on "Does anyone have Nanopore latest updates?"
92% genome coverage of E. coli, average depth of 3.8x. But from just _43_ reads https://github.com/nickloman/massive-nanopore-silliness http://lab.loman.net/2017/03/09/ultrareads-for-nanopore/2732 days ago
- +3 more Comments
