Latest
News
Jobs
Tutorials
Forum
Tags
About
FAQ
Community
Planet
New Post
Log In
New Post
Latest
News
Jobs
Tutorials
Forum
Tags
Planet
Users
Log In
Sign Up
About
Limit : all time
all time
today
this week
this month
this year
0 results • Page
1 of 1
Sort: Rank
Rank
Views
Votes
Replies
Topic does not exist.
No posts found.
0 results • Page
1 of 1
Recent Votes
Comment: Phylogenetic tree of gene clusters
Phylogenetic tree of gene clusters
Answer: Existing Glycomics/Glycan databases with sugar modifications?
Answer: BioMart servers down again...
Comment: In need of help with grad school genomic analysis project
Comment: Assessing read support for coding sequences predicted by TransDecoder
Answer: BioMart servers down again...
Recent Locations •
All
VIB, Ghent, Belgium,
just now
South Korea,
1 minute ago
Ramat Gan,
2 minutes ago
Bergen, Norway,
2 minutes ago
London, UK,
4 minutes ago
Albertslund Municipality,
5 minutes ago
Villefranche-Sur-Saône,
7 minutes ago
Recent Awards •
All
Oracle
to
Nicolas Rosewick
9.4k
Scholar
to
bernatgel
★ 2.9k
Teacher
to
Jean-Karim Heriche
24k
Guru
to
Joe
19k
Teacher
to
Michael Dondrup
48k
Teacher
to
EagleEye
6.8k
Teacher
to
SteveL
▴ 80
Recent Replies
Comment: Extracting variant counts from Gnomad genome VCFs
by
storm1907
• 0
without headers and GT, GQ etc. values ![enter image description here][1] [1]: /media/images/637caf6b-5a2f-4412-b778-6376a3ba
Comment: Extracting variant counts from Gnomad genome VCFs
by
Pierre Lindenbaum
135k
what is "a file like this" ? how is it different from a "normal VCF" ?
Comment: Tool to find chromosome specific repeats
by
Michael Dondrup
48k
Thanks for accepting my answer. Coming back to the initial task of coloring chromosomes I have the impression that you want to do [multicol…
Comment: Next Generation Sequencing: in which sequencing technology the read can Not exce
by
lieven.sterck
11k
I see , but then also Sanger should be able to do this, no? Likely pacbio & nanopore not as the first needs a polymerase to function (and…
Comment: Reference for Salmon
by
ponganta
▴ 180
Hi, I have a question: does the result consist of predicted CDS? Because I was wondering whether you can use predicted CDS instead of e.g. …
Comment: Assessing read support for coding sequences predicted by TransDecoder
by
ponganta
▴ 180
Yes, they were the only problem encountered. However, I did not use the entire RefSeq-database for annotation, but only one custom database…
Comment: problem in creating an object for a list of fasta files
by
cpad0112
15k
If this is bash script, this is unnecessarily complex. Let us say you have all the fasta files in `test` directory, want to use `ls` for l…
Comment: File conversion from coordinates to genes
by
storm1907
• 0
Hello, also I was wondering, if it possible to write gene names together with SNP position as well in the 2nd column?
Answer: BioMart servers down again...
by
Michal @Ensembl
▴ 110
Hi, I'm sorry that you've had a problem while using BioMart. BioMart experienced a heavy load yesterday's evening due to a number of large…
Comment: How Do Heterozygotes And Somatic Mutations Manifest In Sequencing Projects
by
ginnyli056
• 0
How to explain a het (0/1) somatic mutation in tumor with VAF higher than 50%? I saw some of these cases in the TCGA vcf files. could it be…
Answer: Existing Glycomics/Glycan databases with sugar modifications?
by
Joe
19k
Answering my own question (but not in a remotely exhaustive or even particularly thorough manner 😅): - https://unicarb-db.expasy.org/ …
Comment: In need of help with grad school genomic analysis project
by
qmarulfiz
▴ 50
I am new in bioinformatic (just involve for about 3 month) Everything you wrote till the GSEA analysis is similar to my initial plan for t…
Comment: Haplotype Calling Using GATK HaplotypeCaller to Get Exact 35718025 Positions/Loc
by
Pierre Lindenbaum
135k
what is an "accession" ?
Comment: Annotating a genome using a previous annotation file
by
Juke34
★ 5.5k
See table5 of this paper: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6450745/ (Whole-Genome Alignment and Comparative Annotation) Lif…
Comment: Next Generation Sequencing: in which sequencing technology the read can Not exce
by
shelkmike
▴ 420
Illumina sequencing machines don't always add "A". I saw more or less random sequences after the adapter. I wasn't able to understand how I…
Traffic: 2328 users visited in the last hour
Content
Search
Users
Tags
Badges
Help
About
FAQ
Access
RSS
API
Stats
Use of this site constitutes acceptance of our
User Agreement and Privacy Policy
.
Powered by the
version 2.3.6