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1,000 results • Page
4 of 20
Sort: Views
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Views
Votes
Replies
3
votes
1
reply
2.5k
views
News:
Ngs Session At Biocomp Bg 2012 Conference!
next-gen-sequencing
updated 5 weeks ago by
Ram
38k • written 10.9 years ago by
ve9
▴ 50
6
votes
0
replies
2.5k
views
News:
Broad Releases Fastg Multiple Seq Assembly Format
FASTG
reference-format
updated 4 weeks ago by
Ram
38k • written 10.3 years ago by
William
★ 5.2k
8
votes
1
reply
2.5k
views
News:
An Interesting Article On Bioinformatics Education With Some Press For Biostar
meta
biostars
updated 6 weeks ago by
Ram
38k • written 9.7 years ago by
Mary
11k
3
votes
0
replies
2.5k
views
News:
Bioinformatics Specialization on Coursera
MOOCs
Education
updated 5 months ago by
Ram
38k • written 7.6 years ago by
phcompeau
▴ 50
2
votes
1
reply
2.5k
views
News:
Workshop: Programming For Evolutionary Biology
programming
RNA-seq
updated 4 weeks ago by
Ram
38k • written 10.2 years ago by
David Langenberger
9.9k
6
votes
0
replies
2.5k
views
News:
New Methods Section In Plos Computational Biology
publications
plos
updated 4 weeks ago by
Ram
38k • written 10.1 years ago by
Casey Bergman
18k
1
vote
0
replies
2.4k
views
News:
Genomic Data Visualization and Interpretation Workshop
R
Bioconductor
GenVisR
ggplot
RNA-Seq
News
5.7 years ago by
carlopecoraro2
★ 2.3k
11
votes
13
replies
2.4k
views
News:
Ensembl datacentre shut-down: Friday 26th August - Tuesday 30th August 2016
Ensembl
Maintenance
News
6.6 years ago by
Ben_Ensembl
★ 2.2k
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
1
reply
2.4k
views
News:
Advanced Course: R programming and development 15-16. January 2015 (Thursday-Friday), EMBL Heidelberg
programming
course
R
updated 18 days ago by
Ram
38k • written 8.4 years ago by
Laurent
★ 1.7k
4
votes
5
replies
2.4k
views
News:
Kover will provide support via Biostars
kover
kmer
machine learning
news
News
updated 6.2 years ago by
hfan22
▴ 40 • written 6.8 years ago by
Alexandre Drouin
▴ 90
3
votes
1
reply
2.4k
views
News:
The 2014 Nucleic Acids Research Database Issue
database
updated 26 days ago by
Ram
38k • written 9.2 years ago by
Pierre Lindenbaum
153k
6
votes
2
replies
2.4k
views
News:
RNA-Seq Data Analysis Workshop in Berlin, Germany (full)
RNA-Seq
workshop
NGS
data analysis
News
6.3 years ago by
David Langenberger
9.9k
6
votes
0
replies
2.4k
views
News:
http://crackingthebiocode.github.io : Profiles of Computational Biologists & Bioinformaticians
career
updated 18 days ago by
Ram
38k • written 8.5 years ago by
Pierre Lindenbaum
153k
6
votes
1
reply
2.4k
views
News:
The Art of Bioinformatics Scripting. A new book in the Biostar Handbook collection.
education
updated 2.5 years ago by
ghazala.bif.2k18
• 0 • written 3.4 years ago by
Istvan Albert
97k
7
votes
4
replies
2.4k
views
News:
Boston Ma Us Area Folks: Software Carpentry Workshop For Women In Science Coming Up
python
training
updated 4 weeks ago by
Ram
38k • written 10.0 years ago by
Mary
11k
0
votes
0
replies
2.4k
views
News:
Thinking of learning Linux/Python?
next-gen
sequencing
snp
genome
News
updated 6.5 years ago by
GenoMax
127k • written 6.5 years ago by
carlopecoraro2
★ 2.3k
2
votes
1
reply
2.4k
views
News:
RNAseq data analysis with R/ Bioconductor - ONLINE COURSE
R
RNA-Seq
Bioconductor
News
3.0 years ago by
carlopecoraro2
★ 2.3k
3
votes
2
replies
2.4k
views
News:
Samtools/htslib v1.2 released
htslib
samtools
bcftools
updated 12 days ago by
Ram
38k • written 8.1 years ago by
Devon Ryan
103k
2
votes
0
replies
2.4k
views
News:
Summer School in Bioinformatics & NGS Data Analysis
NGS
dnaseq
rnaseq
chipseq
summer shool
News
6.8 years ago by
Leszek
4.2k
8
votes
0
replies
2.4k
views
News:
De Novo Genome Assembly Using Next-Generation Sequence Data (8 - 10 February 2016)
Assembly
Workshop
DNA-Seq
updated 6 months ago by
Ram
38k • written 7.5 years ago by
David Langenberger
9.9k
1
vote
1
reply
2.4k
views
News:
Benefits of DNA Testing - Xcode Life sciences provides preventive healthcare solution
personal-genomics
genetic-testing
updated 11 weeks ago by
Ram
38k • written 7.8 years ago by
sabitha
• 0
3
votes
6
replies
2.4k
views
News:
Brief Getting Started with Broad Firecloud tutorial posted
RNA-Seq
News
6.7 years ago by
Sean Davis
26k
10
votes
4
replies
2.3k
views
News:
Ensembl 77 is out
ensembl
updated 14 months ago by
Ram
38k • written 8.5 years ago by
Emily
23k
20
votes
3
replies
2.3k
views
News:
Nature Comment: Core services: Reward bioinformaticians
career-path
updated 9 months ago by
Ram
38k • written 8.0 years ago by
rtliu
★ 2.2k
2
votes
0
replies
2.3k
views
News:
Connecting NGS Researcher Directly to Data Analysis Provider: New Genohub Service Launched
NGS-data-analysis
bioinformatics-services
updated 21 days ago by
Ram
38k • written 8.9 years ago by
support
▴ 640
6
votes
1
reply
2.3k
views
News:
FastQC Version 0.11.1 released
genome
next-gen-sequencing
updated 21 days ago by
Ram
38k • written 8.8 years ago by
rtliu
★ 2.2k
1
vote
0
replies
2.3k
views
News:
Course: Gene set enrichment and pathway analysis in R . Berlin 12-16 March 2018
Gene
PathwayAnalysis
R
News
5.4 years ago by
carlopecoraro2
★ 2.3k
0
votes
0
replies
2.3k
views
News:
Apply to Penn State's Online Graduate Certificate in Applied Bioinformatics
learn-bioinformatics-online
genome-sequencing
updated 7 months ago by
Ram
38k • written 7.3 years ago by
fiochettal
▴ 10
0
votes
2
replies
2.3k
views
News:
PART FUNDED SCHOLARSHIPS - Coding, data management, and Shiny applications using RStudio for evolutionary biologists and ecologists - May 2017
R
Rstudio
Shiny apps
News
6.0 years ago by
oliverhooker
▴ 110
2
votes
6
replies
2.3k
views
News:
Master in integrated systems biology / Luxembourg
Master course
bioinformatics
systems biology
News
5.7 years ago by
Rainer
▴ 130
2
votes
2
replies
2.3k
views
News:
Interview Dealing with RADseq data: some tips from our instructors
RADseq
NGS
Bioinformatics
News
updated 5.4 years ago by
Istvan Albert
97k • written 5.4 years ago by
carlopecoraro2
★ 2.3k
3
votes
1
reply
2.3k
views
News:
Variathon V0.1 - 2013 - Comparing Existing Or New Pipelines For Variant Calling In Terms Of Accuracy And Efficiency
ngs
conference
updated 4 weeks ago by
Ram
38k • written 10.1 years ago by
Pierre Lindenbaum
153k
3
votes
0
replies
2.3k
views
News:
Workshop: GATK Best Practices for Variant Discovery, Edinburgh, 17-19 July 2017
GATK
workshop
variant calling
News
6.0 years ago by
Bert Overduin
★ 3.7k
25
votes
7
replies
2.3k
views
6 follow
News:
Who qualifies to be a bioinformatician?
resume
bioinformatician
vc
updated 8 months ago by
Ram
38k • written 7.9 years ago by
Pierre Lindenbaum
153k
14
votes
11
replies
2.3k
views
6 follow
News:
Announcing bioSyntax: Syntax highlighting for biological files
bioinformatics
computational biology
News
updated 4.9 years ago by
ababaian
▴ 50 • written 5.2 years ago by
anicet.ebou
▴ 170
0
votes
5
replies
2.3k
views
News:
Workshop: Data manipulation and visualization with Python
next-gen
sequence
genome
SNP
News
6.4 years ago by
carlopecoraro2
★ 2.3k
0
votes
0
replies
2.3k
views
News:
Nature Genetics - DNA Methyloma Analysis in Burkitt and follicular lymphomas
workshop
NGS
epigenetics
epigenomics
updated 15 months ago by
Ram
38k • written 7.5 years ago by
David Langenberger
9.9k
15
votes
4
replies
2.3k
views
News:
Call For Nominations: 2013 Benjamin Franklin Award
benjamin-franklin-award
award
updated 4 weeks ago by
Ram
38k • written 10.1 years ago by
Pierre Lindenbaum
153k
0
votes
0
replies
2.3k
views
News:
Total RNA Commercial Kit Comparison Study
microarray
NGS
RNA-Seq
qPCR
updated 18 days ago by
Ram
38k • written 8.3 years ago by
andorjkiss
▴ 40
1
vote
0
replies
2.3k
views
News:
Genetic data analysis/exploration using R
R
snp
RNA-Seq
data analysis
News
6.0 years ago by
oliverhooker
▴ 110
2
votes
0
replies
2.3k
views
News:
Primer-BLAST can now design primers for a group of related target sequences!
primer-blast
blast
updated 6 weeks ago by
Ram
38k • written 2.5 years ago by
GenoMax
127k
3
votes
0
replies
2.3k
views
News:
Samtools/htslib/bcftools 1.1 released
htslib
samtools
updated 19 days ago by
Ram
38k • written 8.5 years ago by
Devon Ryan
103k
2
votes
0
replies
2.2k
views
News:
Course: Applied Statistics and Bioinformatics with R and Bioconductor. (Berlin, 22-26 January 2018)
Statistics
R
BioCounductor
Bioinformatics
News
5.5 years ago by
c.pecoraro3486
▴ 20
4
votes
0
replies
2.2k
views
News:
2nd UK Bioinformatics Student Symposium on 7 Oct '15 at TGAC, Norwich
symposium
updated 5 months ago by
Ram
38k • written 7.6 years ago by
sayonidas03
▴ 100
6
votes
2
replies
2.2k
views
News:
Interested in de novo transcriptome assembly using Trinity? Check out our interview to Brian Haas
rna-seq
alignment
RNA-Seq
News
6.1 years ago by
carlopecoraro2
★ 2.3k
8
votes
8
replies
2.2k
views
News:
Coronavirus Genome Analysis: a new volume in the Biostar Handbook
biostar handbook
bioinformatics
education
News
written 3.1 years ago by
Istvan Albert
97k
13
votes
8
replies
2.2k
views
News:
NCBI is going to eliminate GI identifiers
GI
number
identifier
ncbi
News
7.0 years ago by
Anima Mundi
★ 2.9k
0
votes
0
replies
2.2k
views
News:
WORKSHOP - Landscape genetic data analysis using R
R
genome
RNA-Seq
News
6.0 years ago by
oliverhooker
▴ 110
0
votes
0
replies
2.2k
views
News:
Intro to Python for Biologists
RNA-Seq
SNP
next-gen
News
5.4 years ago by
oliverhooker
▴ 110
1,000 results • Page
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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
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Recent Replies
Comment: split fasta file to train deep learning model
by
shenwei356
7.9k
Excluding sequences containing any letter not belonging to the 20 [amino acids letters](https://github.com/shenwei356/bio/blob/master/seq/a…
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…
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