Latest
Open
Jobs
Tutorials
Tags
About
FAQ
Community
Planet
New Post
Log In
New Post
Latest
Open
News
Jobs
Tutorials
Forum
Tags
Planet
Users
Log In
Sign Up
About
Limit : this week
all time
today
this week
this month
this year
18 results • Page
1 of 1
Sort: Rank
Rank
Views
Votes
Replies
0
votes
0
replies
22
views
News:
The Canadian Bioinformatics Workshops are back for summer 2023
CBW
training
workshop
2 hours ago by
bioinformatics.ca
• 0
0
votes
0
replies
62
views
News:
Next-Generation Sequencing Data Analysis: A Practical Introduction (May 3-5, 2023 in Munich, Germany)
NGS
DNA-Seq
calling
RNA-Seq
workshop
variant
10 hours ago by
David Langenberger
9.9k
1
vote
0
replies
149
views
News:
NCBI's IgBLAST version 1.21.0 is now available
IgBLAST
BLAST
T-Cell
NCBI
receptors
updated 3 days ago by
GenoMax
127k • written 3 days ago by
PeterC_NCBI
▴ 210
0
votes
0
replies
143
views
News:
ISMB-affiliated virtual tutorial on Neo4j/Cypher for life sciences
neo4j
cypher
graph
knowledge
4 days ago by
Stephen
• 0
0
votes
0
replies
125
views
News:
Announcing workshop on Declarative Programming in Biology and Medicine (Seattle, Sept. 2023)
medicine
declmed
declarative
icfp
precision
4 days ago by
Stephen
• 0
0
votes
0
replies
92
views
News:
Course live online Introduction to Bayesian Analyses using R, May 8th-12th, 2023
bayesian
RProject
course
online
5 days ago by
Sole
• 0
0
votes
0
replies
103
views
News:
course - Reproducibility in Bioinformatics
Docker
Reproducibility
updated 4 days ago by
Ram
38k • written 6 days ago by
carlopecoraro2
★ 2.3k
0
votes
0
replies
457
views
News:
Training in Variant Analysis @NIH, January 28-31, 2020
Variant-Calling
next-gen
genome
updated 4 days ago by
Ram
38k • written 3.3 years ago by
AABI
▴ 130
4
votes
0
replies
753
views
News:
The BioCompute Object App-a-thon starts on May 14!
standards
computation
pipeline
updated 6 days ago by
Ram
38k • written 3.9 years ago by
stephens_sarah
▴ 150
1
vote
0
replies
785
views
News:
Training in Variant Analysis @NIH, USA, April 16-19,2019
genotype
phenotype
updated 4 days ago by
Ram
38k • written 4.1 years ago by
AABI
▴ 130
0
votes
0
replies
953
views
News:
Bioinfo-Core Conference Call, February 6th, 2018 (11 am EST USA and corresponding local times around the world)
bioinformatics-core
bioinfo-core
updated 6 days ago by
Ram
38k • written 5.2 years ago by
GenoMax
127k
5
votes
3
replies
1.3k
views
News:
Bioinfo-Core Conference Call, October 17, 2017 (11 am EDT USA, local times around world)
bioinfo-core
updated 6 days ago by
Ram
38k • written 5.6 years ago by
GenoMax
127k
0
votes
0
replies
1.3k
views
News:
Webinar: Detailed understanding of NGS quality control and file formats
NGS
fastqc
Quality-control
updated 5 days ago by
Ram
38k • written 6.3 years ago by
Persistent LABS
▴ 750
2
votes
2
replies
2.4k
views
News:
ENCODE 2015: Research Applications and Users Meeting
workshop
mouse-encode
encode
updated 6 days ago by
Ram
38k • written 7.8 years ago by
Alex Reynolds
34k
5
votes
0
replies
1.2k
views
News:
Bioconductor 2015 conference live tweeting and materials
bioconductor
R
updated 3 days ago by
Ram
38k • written 7.7 years ago by
Sean Davis
26k
5
votes
0
replies
1.5k
views
News:
New Bioconductor F1000Research Channel for publishing Bioconductor workflows
bioconductor
reproducible-research
updated 3 days ago by
Ram
38k • written 7.7 years ago by
Sean Davis
26k
2
votes
0
replies
2.2k
views
News:
The NAR annual Web Server Issue is here..
web-servers
updated 6 days ago by
Ram
38k • written 7.7 years ago by
Antonio R. Franco
★ 5.0k
6
votes
1
reply
1.7k
views
News:
Are protein domains indivisible?
Athropy
Domains
Proteins
updated 6 days ago by
Ram
38k • written 7.8 years ago by
Deepak Tanwar
★ 4.2k
18 results • Page
1 of 1
Recent Votes
smoothing or binning bigWig file
List of Ongoing and Planned Long Read Sequencing studies?
Are We Rude/Do We Expect Too Much From People Asking Questions On This Forum?
Answer: Read lengths greater than insert length
A: Changing Output From Gene ID to Symbol When Running findMarkers from Scran
Answer: BLAST Database error: No alias or index file found for nucleotide database
Answer: How to get gene from PSIBLAST resuts
Recent Locations •
All
USA,
1 minute ago
South Korea,
5 minutes ago
China,
5 minutes ago
United States,
6 minutes ago
United States,
6 minutes ago
United States,
8 minutes ago
Hong Kong,
8 minutes ago
Recent Awards •
All
Popular Question
to
samuel
▴ 200
Teacher
to
GenoMax
127k
Supporter
to
Daniel
• 0
Popular Question
to
Anand Rao
▴ 550
Popular Question
to
Alex S
▴ 20
Scholar
to
i.sudbery
16k
Teacher
to
AtenaLia
▴ 30
Recent Replies
Comment: split fasta file to train deep learning model
by
pinheirofabiano
▴ 10
@shenwei356, thank you very much for your help, perfect! But now I realized that some fasta sequences contain the letter "B", which is ou…
Comment: Most efficient way to run Diamond against a very very large database (i.e., NCBI
by
Mensur Dlakic
★ 23k
I think it depends on the speed of your local disks and the memory amount. On a single node, breaking up the database doesn't sound like a …
Comment: Sample size for population genetics
by
Jeremy Leipzig
21k
Other populations just make the model harder to generalize, not easier.
Comment: Are We Rude/Do We Expect Too Much From People Asking Questions On This Forum?
by
Vincent Laufer
★ 2.5k
i think there is some of that - my most upvoted comment of all time was a dismissive comment i made while extremely tired. for context i ha…
Comment: Molecular biologist / clinical pharmacologist (f/m/d)
by
Jeremy
▴ 770
Is this job on site in Vienna or remote?
Comment: smoothing or binning bigWig file
by
rls_08
▴ 40
if you use bigwigCompare , that would not create a sliding window, but instead, it will output the mean for each bin, according to the -bin…
Comment: Sample size for population genetics
by
zimmer.schweiz
• 0
Thank you so much for your answer. For common polygenic diseases, would it make sense to increase the number of populations sampled, in ord…
Answer: Sample size for population genetics
by
Jeremy Leipzig
21k
For a rare penetrant monogenic disease? A few cases. For a common polygenic disease or trait? 500k-10M
Answer: using GRanges metadata to constrain overlap searches between objects
by
seidel
11k
Rather than do all overlaps all the time for all samples, why not restrict the data by sample when you can. The code below works about 4 ti…
Comment: How to get gene from PSIBLAST resuts
by
Tom
• 0
Hello, thank you for your answer, I have a question, Why the information from the GFF file and from the feature table is different? I see …
Comment: SNP ID (rsID) to Chr no. and Position
by
Jewahir
• 0
Yeah, thank you for that!!
Comment: 1000 genomes hg38 with dbSNP rsid
by
Ram
38k
It should be pretty straightforward. Just to save you some pain, run these on the 1000g VCF once you download it: 1. `vt decompose -s` to …
Comment: 1000 genomes hg38 with dbSNP rsid
by
Vince
▴ 150
Yeah, I had some hope that I wouldn't need to mess with doing this ...
Answer: counting the unmapped reads
by
chemkhi.ali13
• 0
> Hi all, > > I have a sam file, my supervisor asked me to count the number of > unmapped reads, which command I should use? > > sam…
Comment: 1000 genomes hg38 with dbSNP rsid
by
Ram
38k
In that case, you'll need to get the VCF from 1000g - that's probably going to be the only place where individual level data is available, …
Traffic: 1617 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