3943 days ago
Bioinformatics PhDs - Cover Letter
OverviewThe reception your cover letter will receive is more varied and unpredictable...professional, and, perhaps more to the point, Yale rarely "comes calling." An e...l that cares only about your teaching (increasingly rare), a...3364 days ago
RNA Sequencing Helps Identify Functional Variants from GWAS
For Alzheimer’s and other complex disorders, mining the genome for disease-associated variants is no longer the obstacle. Th...3814 days ago
3651 days ago
2795 days ago
Genome Assembly Tools and Software - PART2 !!
The genome assemblers generally take a fi...Detection and Assembly of Insertion VariantsMindTheGap is a software...ection and assembly of DNA insertion variants in NGS read datasets with res...ses a simple error correction, viral variants assembling based on maximum-b...2683 days ago
3940 days ago
List of bioinformatics open source projects/software.
Open source software is software that can be freely use...p://www.gene-talk.de/ Tool for filtering sequence variants in VCF files. Network for sci...exchange. Database of annotations aboute sequence variants with clinically relevant info...3755 days ago
3544 days ago
3623 days ago
Structural polymorphism analysis from NGS data
The LabEx BASC (Biodiversity, Agroecosystems, Society, Climate), a network of 13 la...idate will be in charge of the detection of polymorphisms including structural variants, of the comparison of multipl...3946 days ago
3946 days ago
3878 days ago
3556 days ago
3871 days ago
Dr. Ken Buetow: IS & Personalized Medicine Lecture-Part 1
Full Lecture Abstract Creating an Evidence Engine to S...oped. These technologies identify the millions of variants present in normal individuals...fficiently and accurately computationally identify variants. More recently, the analyti...3868 days ago
2073 days ago
Samtools commands for bioinformatician !
## count mapped reads samtools view -c -F 260 mapping_...x sal_sej_sorted.bam.bam ### identifying genome variants (mpileup command) # -g : out...els # -c : find snp # -v : output only potential variants bcftools view -c -v sal_vars...1601 days ago
3951 days ago