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Tool: Dgidb - Mining The Druggable Genome

tool database dgidb interaction gene drug written 4.8 years ago by Obi Griffith ♦ 16k

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Tool: Dgidb - Mining The Druggable Genome

tool database dgidb interaction gene drug written 4.8 years ago by Obi Griffith ♦ 16k • updated 3.6 years ago by Malachi Griffith ♦ 16k

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Recent Replies

A: Understanding Annovar Output by h.mon ♦ 16k
There is an ANNOVAR intro here: [Introduction to VCF file and some of its complications][1] And...
A: Understanding Annovar Output by newbinf • 0
I realize that DP:RD:AD is total reads: reference allele reads: alternative allele reads. Please...
A: Is Position In Vcf File 1-Based (First Index Is At 1 Not 0)? by Shicheng Guo • 5.0k
Just remember no matter 0 based or 1 based, the later number will be the position for that base, ...
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I am trying to call SNPs and indels, but all the tools I found are compatible with bam files gene...
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Okay. `MyOutcomeTrait` is the variable that you're modelling, i.e., the `y` variable. For exampl...
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`--recode12` is no the same. The Illumina AB format is quite specific, often called *TOP / BOT* f...
C: genome sequence look up tool by evcon • 0
Thanks! This is perfect! Knew this had to exist already.
C: miRNA-seq Trimmomatic adapter file by WouterDeCoster ♦ 30k
I have adapted your title to make it more explicit.
A: SNP Analysis on Single Cell Data from 10x by droseeee • 0
Hi, I am attempting to do the same. Has anyone figured out a method with R? Thanks!!
A: genome sequence look up tool by h.mon ♦ 16k
[BioPython][1] and [pyfaidx][2] in python, [samtools][3] on the command-line [1]: https://bio...
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search this site for "samtools faidx" and the related python libraries (pyfaidx)
A: strelka2 vs strelka1 by sbilobram • 10
In both cases configureStrelkaSomaticWorkflow.py is run with matched normal and tumour bams and ...

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