aquaria Posts

Latest

Open

RNA-Seq

ChIP-Seq

SNP

Assembly

Tutorials

Tools

Jobs

Forum

Planet

All »

Home

Welcome to Biostar! about • faq • rss

Community

Log In

Sign Up

Add New Post

Showing: aquaria • reset

or Classic search

votes

answers

2.9k

views

answers

Tool: Aquaria: simplifying discovery and insight from protein structures

snp tool sequence aquaria 3d structure written 4.1 years ago by Aquaria team • 90

Recent Votes

Recent Locations • All »

EMBL-EBI, 1 minute ago
Helsinki, 1 minute ago
Germany, 2 minutes ago
European Union, 2 minutes ago
Uruguay, 2 minutes ago
European Union, 2 minutes ago
United Kingdom, 3 minutes ago

Recent Awards • All »

Teacher to Kevin Blighe ♦ 37k
Teacher to WouterDeCoster ♦ 36k
Teacher to Pierre Lindenbaum ♦ 117k
Appreciated to Ben_Ensembl • 940
Great Question to jaqx008 • 40
Teacher to Pierre Lindenbaum ♦ 117k

Recent Replies

C: help with python homework assignments by finswimmer ♦ 10k
Hello https://www.biostars.org/u/52730/ , please use the `ADD REPLY`button below the post you li...
C: How to check the presence of mutations of a specific gene in a specific VCF file by Davide Chicco • 70
Alright, thanks. First of all, my VCF files are in the hg19 coordinates, therefore they are diffe...
A: help with python homework assignments by katerinaxe87 • 10
Hello! I apologize perhaps i expressed myself wrong. I have Written my code but i don’t get the r...
C: How to approximate history of SNP by representative selection tests by i.sudbery ♦ 3.8k
These measures are all measures of nucleotide frequency. I'm not sure of the meaning of " time of...
C: Remove duplicate readnames from a bam file by Bastien Hervé ♦ 3.3k
I'll add this one https://gatkforums.broadinstitute.org/gatk/discussion/7431/markduplicates-erro...
C: Remove duplicate readnames from a bam file by finswimmer ♦ 10k
Hello https://www.biostars.org/u/52753/ , have you tried the things mentioned in https://www.bio...
C: Identify cell types based-on RNA-seq/ChIP-seq data by dcheng1 • 0
I will try that. Thanks!!
C: VEP vs webserver Polyphen scores by F • 3.3k
Sorry to be this much disturbing, I have likely annotated my .vcf files (SNV) with Vep just by d...
C: Oncodriveclust R Package by F • 3.3k
OncodriveCLUIST has been updated with OncodriveCLUSTL https://bitbucket.org/bbglab/oncodriveclus...
C: running BUSCO on unknown genomes ? by Corentin • 250
I do not think you can skip Augustus. The default parameter depends on the lineage you choose (c...
C: dNdScv error: Zero coding substitutions found in this dataset by F • 3.3k
Thank you very much > print(head(sel_cv), digits = 3) gene_name n_syn n_mis n_...
C: how i can separate mitochondrial sequences from chromosomal sequences by WouterDeCoster ♦ 36k
Please elaborate on the data you have and how you obtained it.

Content

Help

About
FAQ

Access

RSS
Stats
API

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.

Traffic: 2183 users visited in the last hour