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127 results • Page
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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
0
votes
0
replies
448
views
News:
Live webinar (Feb 12 at 12PM Eastern): variant calling for bench scientists
variant-calling
wgs
wes
updated 13 days ago by
Ram
38k • written 3.1 years ago by
Basepair
• 0
0
votes
2
replies
1.4k
views
News:
M.Phil Program in Bioinformatics
education
career
updated 10 days ago by
Ram
38k • written 7.4 years ago by
rrojha143
• 0
0
votes
9
replies
1.9k
views
News:
Practical Genomics: From Biology to Biostatistics Workshop (Baltimore, MD)
workshop
updated 21 days ago by
Ram
38k • written 8.7 years ago by
Matt Shirley
10k
0
votes
0
replies
134
views
News:
Course - GENERALIZED LINEAR MODELS in R
GLMs
R
GeneralisedLinearModels
20 days ago by
carlopecoraro2
★ 2.3k
0
votes
0
replies
1.3k
views
News:
Free Ensembl webinar
Ensembl
updated 18 days ago by
Ram
38k • written 8.5 years ago by
Emily
23k
0
votes
0
replies
2.1k
views
News:
Conference Announcement - Camda 2014
conference
updated 24 days ago by
Ram
38k • written 9.1 years ago by
okko.clevert
▴ 240
0
votes
0
replies
2.6k
views
News:
Call-for-Papers in Epigenomics (BMRI, impact factor 2.7)
epigenomics
papers
updated 18 days ago by
Ram
38k • written 8.5 years ago by
benoukraf
• 0
0
votes
0
replies
159
views
News:
course - single-cell RNAseq with R/Bioconductor
Bioconductor
single-cell
genomics
RNAseq
updated 20 days ago by
Ram
38k • written 4 weeks ago by
carlopecoraro2
★ 2.3k
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
0
votes
0
replies
1.6k
views
News:
Project Management Tools for Bioinformaticians and Service Providers
Quotation-software
LIMS
Project-management
updated 14 days ago by
Ram
38k • written 8.3 years ago by
support
▴ 640
0
votes
0
replies
1.8k
views
News:
Workshop: Analysis of Massively Parallel Sequencing (NGS) Data
NGS
Data-Analysis
updated 13 days ago by
Ram
38k • written 8.2 years ago by
Samarth Kulshrestha
▴ 270
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
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
120
views
News:
Course - INTRODUCTION TO THE ANALYSIS OF LONGITUDINAL DATA WITH R
Genomics
LongitudinalData
R
27 days ago by
carlopecoraro2
★ 2.3k
0
votes
0
replies
2.1k
views
News:
Second Annual International Environmental Omics conference to be held in Liverpool, UK. September 15th-18th
Conference
updated 21 days ago by
Ram
38k • written 8.7 years ago by
Daniel
★ 3.9k
0
votes
0
replies
27
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
4.6k
views
News:
Bioinformatics Training Courses - Metagenomics and NGS data analysis - Sydney and Canberra, Australia
metagenomics
training
next-gen-sequencing
updated 21 days ago by
Ram
38k • written 8.8 years ago by
Neilfws
49k
0
votes
0
replies
2.7k
views
News:
LAST CALL: Hands-On NGS Data Analysis Workshops 2014
NGS
microRNA
workshop
RNA-Seq
updated 21 days ago by
Ram
38k • written 8.7 years ago by
David Langenberger
9.9k
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
808
views
News:
Training in genomics workflows for computational novices
bash
training
workshop
cloud
updated 13 days ago by
Ram
38k • written 3.8 years ago by
ebecker
• 0
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
0
votes
0
replies
3.5k
views
News:
Journal Of Bioinformatics Research Studies- Call For Papers
publication
biology
updated 21 days ago by
Ram
38k • written 9.0 years ago by
jbrs.editor
• 0
0
votes
2
replies
300
views
News:
Course - Metagenomics, metatranscriptomics, and multi'omics for microbial community Studies
Metagenomics
Metatranscriptomics
Multiomics
updated 10 days ago by
Ram
38k • written 10 days ago by
carlopecoraro2
★ 2.3k
0
votes
0
replies
556
views
News:
FINAL CALL :: Online Course - A Practical Introduction to NGS Data Analysis (July 14-16, 2021)
NGS
workshop
updated 10 days ago by
Ram
38k • written 21 months ago by
David Langenberger
9.9k
0
votes
0
replies
1.8k
views
News:
MinION access program is open
minion
updated 18 days ago by
Ram
38k • written 8.5 years ago by
Istvan Albert
97k
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
127 results • Page
3 of 3
Recent Votes
A: In Seurat, How Do nCount_RNA Differ from nFeature_RNA?
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
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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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