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1,000 results • Page
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Sort: replies
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5
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2
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3.5k
views
News:
Tuesday 10/29 Live Tour Of New Features In Integrated Genome Browser 8
genome-browser
RNA-seq
ChIP-seq
updated 6 months ago by
Ram
40k • written 9.9 years ago by
Ann
★ 2.4k
0
votes
2
replies
3.2k
views
News:
Course: Practical GWAS using Linux and R. 23-27 October 2017, Berlin (Germany)
GWAS
Linux
R
updated 4 months ago by
Ram
40k • written 6.1 years ago by
carlopecoraro2
★ 2.3k
6
votes
2
replies
2.1k
views
News:
Galaxy-specific Biostar Instance
galaxy
biostars
updated 7 months ago by
Ram
40k • written 9.4 years ago by
martenson
▴ 380
2
votes
2
replies
1.5k
views
News:
User-friendly Bioinformatics From RNA Seq to Biological Interpretation
machine-learning
RNA-seq
updated 4 months ago by
Ram
40k • written 5.2 years ago by
sahil
▴ 10
6
votes
2
replies
1.7k
views
News:
Belly Button Biodiversity Project Requests Your Analysis
biodiversity
project
updated 7 months ago by
Ram
40k • written 10.9 years ago by
Mary
11k
7
votes
2
replies
2.1k
views
News:
Upcoming Hands-On Workshop: microRNA Analysis Using Next-Generation Sequencing
NGS
microRNA
workshop
updated 5 months ago by
Ram
40k • written 7.3 years ago by
David Langenberger
10k
0
votes
2
replies
876
views
News:
Online Course - A Practical Introduction to NGS Data Analysis (February 01-03, 2023)
NGS
DNAseq
variant-calling
RNAseq
8 months ago by
David Langenberger
10k
8
votes
2
replies
2.2k
views
News:
The bioinformatics chat is a new podcast about bioinformatics. In the first episode we discuss Scallop, a transcriptome assembler
podcast
Assembly
RNA-Seq
updated 4 months ago by
Ram
40k • written 6.4 years ago by
roma
▴ 120
2
votes
2
replies
2.5k
views
News:
Interview Dealing with RADseq data: some tips from our instructors
NGS
RADseq
updated 4 months ago by
Ram
40k • written 5.9 years ago by
carlopecoraro2
★ 2.3k
1
vote
2
replies
1.6k
views
News:
NCBI Datasets - try it out!
Assembly
refseq
genome
ncbi
updated 3 months ago by
Ram
40k • written 3.5 years ago by
vkkodali_ncbi
★ 3.6k
1
vote
2
replies
1.3k
views
News:
Webinar on Diagnosis of Rare Diseases using NGS Based Multi-gene Testing- Case studies by Dr.Aparna Ganapathy on 18 Apr 2018
variant-calling
rare-disease
dna-seq
strand-ngs
updated 4 months ago by
Ram
40k • written 5.5 years ago by
Genomics
▴ 70
8
votes
2
replies
790
views
News:
Save time and money through improved onboarding of your NGS data scientists
NGS
data-analysis
updated 6 months ago by
Ram
40k • written 3.7 years ago by
David Langenberger
10k
2
votes
2
replies
320
views
News:
NCBI BLAST+ 2.14.1 Now Available
NCBI
BLAST
4 weeks ago by
PeterC_NCBI
▴ 330
2
votes
2
replies
1.9k
views
News:
Briefings In Bioinformatics International, Interdisciplinary, Multi-Level Bioinformatics Training And Education
education
updated 6 months ago by
Ram
40k • written 10.0 years ago by
Pierre Lindenbaum
157k
0
votes
2
replies
565
views
News:
The Practice of RADseq: Population Genomics Analysis with Stacks (RADS02) Early bird deadline approaching - 20th September
population-genomics
radseq
stacks
updated 6 days ago by
Dave Carlson
★ 1.4k • written 7 days ago by
oliverhooker
▴ 110
13
votes
2
replies
1.3k
views
News:
Thank you Biostars!
meta
updated 3 months ago by
Ram
40k • written 4.4 years ago by
Glory Basumata
▴ 140
4
votes
2
replies
2.9k
views
News:
NCBI NOW (Next generation sequencing Online Workshop) October 13 - 23 , 2015
NCBI
DNA-Seq
NGS
RNA-Seq
updated 5 months ago by
Ram
40k • written 8.0 years ago by
rtliu
★ 2.2k
3
votes
2
replies
2.5k
views
News:
Samtools/htslib v1.2 released
htslib
samtools
bcftools
updated 6 months ago by
Ram
40k • written 8.6 years ago by
Devon Ryan
103k
11
votes
2
replies
1.4k
views
News:
ASA discusses limitations of p-values what are the alternatives?
statistics
p-value
updated 5 months ago by
Ram
40k • written 7.5 years ago by
dariober
14k
5
votes
2
replies
1.5k
views
News:
#scRNABIO & organoids meeting
single-cell-sequencing
microfluidics
organoids
updated 4 months ago by
Ram
40k • written 5.1 years ago by
aln
▴ 320
4
votes
2
replies
1.2k
views
News:
Hands-On Workshop: How to use bisulfite-treated sequencing to study DNA methylation (BS-Seq, Bisulfite-Seq, WGBS)
Workshop
methylation
bisulfite
updated 3 months ago by
Ram
40k • written 4.0 years ago by
Lars
★ 1.0k
2
votes
2
replies
1.3k
views
News:
GeNets: a unified web platform for network-based genomic analyses
networks
pathways
RNA-Seq
visualization
updated 4 months ago by
Ram
40k • written 5.3 years ago by
ivivek_ngs
★ 5.2k
1
vote
2
replies
1.6k
views
News:
Workshop: Data analysis in high throughput biology. deadline today (2 places left)
next-gen
R
RNA-Seq
updated 4 months ago by
Ram
40k • written 6.5 years ago by
carlopecoraro2
★ 2.3k
0
votes
2
replies
911
views
News:
Training - Introduction to Deep Learning
Deep-Learning
Machine-Learning
Python-Programming
updated 3 months ago by
Ram
40k • written 3.2 years ago by
carlopecoraro2
★ 2.3k
5
votes
2
replies
4.4k
views
News:
GeneSCF (Gene Enrichment Tool): Advice to users
kegg
GeneSCF
GO
annotation
updated 7 months ago by
Ram
40k • written 6.7 years ago by
EagleEye
7.5k
3
votes
2
replies
1.1k
views
News:
Genome Informatics meeting software list
meetings
genomics
informatics
software
updated 4 months ago by
Ram
40k • written 5.9 years ago by
Sean Davis
26k
3
votes
2
replies
483
views
News:
Participate in a NCBI/NIAID Virtual Codeathon: VCF Files for Population Genomics, Jul 31 - Aug 4, 2023
VCF
SARS-CoV-2
NCBI
Codeathon
4 months ago by
PeterC_NCBI
▴ 330
2
votes
2
replies
818
views
News:
Interested in Machine Learning?
deep-learning
machine-learning
updated 3 months ago by
Ram
40k • written 4.4 years ago by
carlopecoraro2
★ 2.3k
2
votes
2
replies
1.8k
views
News:
Introducing a new Instructor of Physalia-Courses: Dr. January Weiner
next-gen
SNP
sequence
updated 5 months ago by
Ram
40k • written 6.8 years ago by
carlopecoraro2
★ 2.3k
0
votes
2
replies
1.5k
views
News:
Free Webinar: Sequence alignment: the central step in reference based Next Generation Sequencing data analysis
next-gen
SAM
alignment
sangenix
updated 5 months ago by
Ram
40k • written 6.7 years ago by
Persistent LABS
▴ 750
6
votes
2
replies
2.4k
views
News:
Interested in de novo transcriptome assembly using Trinity? Check out our interview to Brian Haas
alignment
RNA-Seq
updated 5 months ago by
Ram
40k • written 6.6 years ago by
carlopecoraro2
★ 2.3k
6
votes
2
replies
968
views
News:
Temporarily reduced functionality of Ensembl and Ensembl Genomes
Ensembl
updated 4 months ago by
Ram
40k • written 4.6 years ago by
Ben_Ensembl
★ 2.3k
0
votes
2
replies
132
views
News:
NGS & Microarray Custom Data Analysis Training Program
snp
RNA-Seq
next-gen-sequencing
ChIP-Seq
updated 3 months ago by
Ram
40k • written 4.2 years ago by
suvarna
• 0
1
vote
2
replies
543
views
News:
Course: Network Analysis in R
NetworkAnalyis
R
8 months ago by
carlopecoraro2
★ 2.3k
1
vote
2
replies
2.2k
views
News:
Workshop: Metagenomics, Metatranscriptomics, and multi'omics for microbial community studies (9-13 April 2018 in Berlin)
Metatranscriptomics
Metagenomics
updated 4 months ago by
Ram
40k • written 5.6 years ago by
carlopecoraro2
★ 2.3k
0
votes
2
replies
1.9k
views
News:
RNA-Seq Data Analysis Workshop in Berlin, Germany (13 - 16 March 2018)
NGS
RNA-Seq
sequencing
updated 4 months ago by
Ram
40k • written 5.7 years ago by
David Langenberger
10k
0
votes
2
replies
652
views
News:
Course - Metagenomics, metatranscriptomics, and multi'omics for microbial community Studies
Metagenomics
Metatranscriptomics
Multiomics
updated 6 months ago by
Ram
40k • written 6 months ago by
carlopecoraro2
★ 2.3k
1
vote
2
replies
938
views
News:
Sage Bionetworks is seeking researchers and data scientists to participate in software user research!
research
software
updated 4 months ago by
Ram
40k • written 4.6 years ago by
duminda.aluthgamage
▴ 30
6
votes
2
replies
2.5k
views
News:
RNA-Seq Data Analysis Workshop in Berlin, Germany (full)
NGS
RNA-Seq
workshop
updated 5 months ago by
Ram
40k • written 6.8 years ago by
David Langenberger
10k
4
votes
2
replies
252
views
News:
Standalone NCBI ClusteredNR database now available for download
ClusteredNR
NCBI
standalone
BLAST
20 days ago by
PeterC_NCBI
▴ 330
0
votes
2
replies
1.3k
views
News:
Webinar on fast and accurate DNA variant calling on 26 Apr 2017
variant-calling
SNP
gatk
strand-ngs
alignment
updated 4 months ago by
Ram
40k • written 6.4 years ago by
Genomics
▴ 70
0
votes
2
replies
1.7k
views
News:
Webinar: Multi-omics: Challenges, opportunities and application to biomarker discovery
biomarker
next-gen-sequencing
multiomics
cancer
updated 4 months ago by
Ram
40k • written 6.2 years ago by
Persistent LABS
▴ 750
1
vote
2
replies
504
views
News:
Gene Set Enrichment Analysis in R/Bioconductor
Gene-Set-Enrichment-Analysis
R
Cancer-Genomics
GSEA
10 months ago by
carlopecoraro2
★ 2.3k
2
votes
2
replies
2.1k
views
News:
De Novo Transcriptome Analysis (Assembly and Differential Gene Expression in Non-Model Organisms)
Assembly
RNA-Seq
updated 5 months ago by
Ram
40k • written 7.2 years ago by
JohnBlue81
▴ 400
1
vote
2
replies
1.2k
views
News:
New chat server (Discord) for bioinformatics
community
8 months ago by
Samuel Lampa
★ 1.3k
1
vote
2
replies
1.5k
views
News:
My own brand-new blog for bioinformatics learning
learning
updated 7 months ago by
Ram
40k • written 5.8 years ago by
Wenhu_Cao
▴ 100
0
votes
2
replies
2.0k
views
News:
Seqnews.Net: Discover And Share News On Next-Generation Sequencing
next-gen-sequencing
updated 7 months ago by
Ram
40k • written 10.8 years ago by
David Langenberger
10k
14
votes
2
replies
5.3k
views
News:
Open Targets, identifying targets for drug development in the treatment of diseases.
database
Drug
open-targets
updated 5 months ago by
Ram
40k • written 7.3 years ago by
Denise CS
★ 5.2k
0
votes
2
replies
1.9k
views
News:
Illumina iSeq 100 sequencer
firefly
illumina
iSeq100
updated 4 months ago by
Ram
40k • written 5.7 years ago by
GenoMax
134k
1
vote
2
replies
1.7k
views
News:
Making efficient NGS data analysis softwares - GATB-Core Library Tutorial
next-gen
GATB
updated 5 months ago by
Ram
40k • written 7.0 years ago by
patrick.durand
▴ 140
1,000 results • Page
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A: In Seurat, How Do nCount_RNA Differ from nFeature_RNA?
How to identify 16s sequences from binning data(contigs)?
geom_signif() uses t-test to compare between more than 3 groups... Isn't this wrong?
Answer: Filter transcription factors
Comment: Calculation of TMB on gene level
Comment: Should I Learn Docker to Run Command Line Bioinformatics Tool?
Comment: ATAC-seq troubleshoot - Just Noise
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Recent Replies
Comment: gene correlations in between two groups
by
ATpoint
76k
And how should I know this? I cannot read minds, nor see your screen, data or anything. Please ask a good question with necessary details. …
Comment: gene correlations in between two groups
by
edus_bioinfo
▴ 40
Thanks. But they are already analyzed. Afaik it analyzes raw data. In my dataset for each gene there is score. I want to interpret the data…
Answer: GWAS phenotype
by
dthorbur
▴ 550
Hello again. Yes, you can conduct GWAS using binary trait data, but it comes with a whole suite of complications. See [this](https://ww…
Comment: geom_signif() uses t-test to compare between more than 3 groups... Isn't this wr
by
RM123
▴ 10
Hello Dariober, That seems like a good solution, however I'm pretty new to R. Could you tell me how I can do that?
Comment: how to create a loop in R
by
Nicolas Rosewick
10k
Not really a bioinformatics related question. Start by looking at R tutorial, there is plenty of them online e.g. : https://www.statmethods…
Comment: Violin plot (Monocle 3) - Troubleshooting
by
fracarb8
★ 1.2k
You did not add the screenshot.
Answer: BED files
by
Alex Reynolds
35k
Generically via `bedmap`: ``` bedmap --echo --echo-map --count exome.bed annotations.bed > answer.bed ``` The `annotations.bed` fil…
Comment: geom_signif() uses t-test to compare between more than 3 groups... Isn't this wr
by
dariober
14k
It seems to me that anova followed by HSD is a more sensible approach than applying independent t-tests. Granted this is the first time I s…
Comment: BED files
by
barslmn
★ 1.8k
I am guessing you want the annotation files. https://ftp.ncbi.nlm.nih.gov/refseq/H_sapiens/annotation/GRCh38_latest/refseq_identifiers/
Comment: Filter human transcription factors
by
Alex Reynolds
35k
Curious how redundant these TFs are. Jeff Vierstra has done some analysis on this to simplify model sets: https://www.vierstra.org/resource…
Comment: Read block operation failed with BAM file
by
Alex Reynolds
35k
https://github.com/samtools/htslib/pull/1676 patches a seek issue in `htslib` (upon which `samtools` and `pysam` depend)
Comment: Merging the filename with tsv files for master file
by
barslmn
★ 1.8k
Could you add samples from your files and your expected output.
Comment: Download an example of fully-imputed VCF files ?
by
barslmn
★ 1.8k
Check out the 1000 genomes project. https://ftp.1000genomes.ebi.ac.uk/vol1/ftp/release/20130502/
Comment: obtaining circular RNAs' sequences from circBase
by
Barry Digby
★ 1.2k
Sorry my mistake! it’s been a minute since I’ve used these sites. Yes that it is common place, what is the goal of your analysis using th…
Comment: gene correlations in between two groups
by
ATpoint
76k
Use specialized software to analyse CRISPR/RNAi data, such as MAGeCK.
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