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750 results • Page
2 of 15
Sort: Votes
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Votes
Replies
7
votes
14
replies
560
views
ggsave() bug in ggplot2?
R
ggplot2
updated 5 days ago by
Ram
39k • written 5 days ago by
Medeea
▴ 10
7
votes
6
replies
259
views
Italicise annotations with pheatmap
R
Pheatmap
updated 12 hours ago by
ATpoint
72k • written 22 hours ago by
jamie.pike
▴ 80
7
votes
2
replies
637
views
Forum:
How to follow a particular post on Biostars?
meta
updated 4 hours ago by
Ram
39k • written 3.5 years ago by
natasha.sernova
★ 3.9k
7
votes
8
replies
960
views
Forum:
Guidelines / Limits for Shared Bioinformatics Support
Core
Shared-Resources
Collaboration
updated 3 hours ago by
Ram
39k • written 3.5 years ago by
Charles Warden
8.2k
7
votes
17
replies
7.3k
views
10 follow
Python FASTA scripting
Python
FASTA
updated 1 day ago by
Ram
39k • written 3.7 years ago by
damonlbp
▴ 20
7
votes
1
reply
223
views
How to plot combined bar graph in R
barplot
R
singleR
ggplot
updated 6 days ago by
Ram
39k • written 13 days ago by
Bioinfo
▴ 20
7
votes
6
replies
2.8k
views
Error: --fst requires at least two nonempty clusters.
Plink
updated 1 day ago by
dre.gaudio
• 0 • written 6.0 years ago by
msimmer92
▴ 300
7
votes
4
replies
392
views
Forum:
[Meta] Use of AI
AI
Artificial-Intelligence
meta
ChatGPT
updated 1 day ago by
Ram
39k • written 3 days ago by
Vincent Laufer
★ 2.9k
6
votes
6
replies
1.1k
views
Want read count with respect to geneID instead of transcript IDs
RNA-Seq
updated 4 hours ago by
Ram
39k • written 3.5 years ago by
archana.bioinfo87
▴ 180
6
votes
5
replies
1.1k
views
7 follow
Forum:
What do you think of sci-hub?
sci-hub
updated 1 hour ago by
Ram
39k • written 3.4 years ago by
cduukj
• 0
6
votes
0
replies
808
views
News:
CWL user support moving to https://cwl.discourse.group/; many thanks to Biostars for over 4 years of support!
cwl
thanks
updated 23 hours ago by
Ram
39k • written 3.6 years ago by
Michael R. Crusoe
★ 1.9k
6
votes
25
replies
29k
views
14 follow
CluserProfiler message "No gene can be mapped"
R
updated 6 days ago by
13554221497
• 0 • written 5.2 years ago by
ARich
▴ 130
6
votes
17
replies
4.5k
views
8 follow
Eigen genes using WGCNA
wgcna
eigengenes
updated 21 hours ago by
chaco001
▴ 40 • written 4.7 years ago by
shivangi.agarwal800
▴ 120
6
votes
7
replies
309
views
NCBI API, Perl
API
NCBI
updated 23 hours ago by
GenoMax
129k • written 1 day ago by
alessandro.alma00
• 0
6
votes
5
replies
712
views
Forum:
Tips on: How to organise data on servers
genotype
warehouse
servers
updated 4 hours ago by
Ram
39k • written 3.5 years ago by
flight505
▴ 90
6
votes
6
replies
142
views
Contigs to chromosomes annotation
Assembly
mapping
contigs
updated 41 minutes ago by
GenoMax
129k • written 13 hours ago by
alexandru.bologa.marian
▴ 50
6
votes
7
replies
3.6k
views
7 follow
Which method is the best for using in "dba.count" in Diffbind R package
ChIP-Seq
diffbind
updated 1 day ago by
Jo
• 0 • written 3.7 years ago by
m.sadman.sakib
▴ 120
6
votes
5
replies
5.3k
views
BWA aln - failed to locate the index
alignment
bwa
updated 3 days ago by
Ram
39k • written 3.7 years ago by
m.wekking
▴ 10
5
votes
7
replies
1.7k
views
How to prevent reduce from being performed in GRanges during setdiff
blunt-end
genomicranges
setdiff
updated 4 days ago by
hossiny
• 0 • written 2.3 years ago by
Bosberg
▴ 50
5
votes
10
replies
2.8k
views
7 follow
Job:
Bioinformatics tutor good in Python
python
updated 6 days ago by
Ram
39k • written 4.1 years ago by
Yes_peter
▴ 10
5
votes
0
replies
998
views
Job:
Postdoctoral Scientist (Bioinformatics) at The Earlham Institute, UK
genome
methylation
sequencing
updated 5 days ago by
Ram
39k • written 3.9 years ago by
El Blanco
▴ 40
5
votes
2
replies
731
views
News:
The precisionFDA BioCompute Object App-a-thon has been extended to October 18!
BioCompute
challenge
updated 5 days ago by
Ram
39k • written 3.9 years ago by
hollystephens723
▴ 70
5
votes
3
replies
712
views
Forum:
price of MSI detection by NGS for 1 person
next-gen
updated 5 days ago by
Ram
39k • written 3.9 years ago by
jandoubi.nouha333
▴ 20
5
votes
6
replies
444
views
Inquiry Regarding Somatic Analysis and Normal Sample Requirement
ngs
somatic
germline
updated 6 days ago by
Ram
39k • written 14 days ago by
Nour-eddine
▴ 30
5
votes
3
replies
4.0k
views
What Do Chromosome Codes Such As 'Chr_Random' Represent?
plink
chromosome
updated 6 days ago by
Ram
39k • written 10.8 years ago by
zhuwei.cug
▴ 30
5
votes
7
replies
269
views
Alignment of case vs. control from different origin
Alignment
RNAseq
updated 9 hours ago by
i.sudbery
17k • written 6 days ago by
sativus
• 0
5
votes
2
replies
209
views
How to detect specific genes in metagenomics data
metagenomics
genes
updated 5 days ago by
Ram
39k • written 5 days ago by
aziznasr1920
▴ 10
5
votes
5
replies
2.0k
views
Forum:
BCL files as deliverables from a sequencing center
core-facility
service-provider
updated 6 days ago by
Ram
39k • written 4.0 years ago by
Ido Tamir
5.2k
5
votes
2
replies
1.0k
views
Forum:
ISMB bioinfo-core workshop call for lightning talks
conferences
updated 6 days ago by
Ram
39k • written 4.1 years ago by
Madelaine Gogol
5.3k
5
votes
5
replies
1.4k
views
Improve illumina short read assembly using PacBio long reads
Assembly
Illumina
genome
PacBio
updated 6 days ago by
Ram
39k • written 4.0 years ago by
shachigahoimbi
▴ 20
5
votes
3
replies
1.1k
views
Introduction to Structural Bioinformatics
protein
structural-bioinformatics
updated 5 days ago by
Ram
39k • written 4.0 years ago by
iamakhilverma
• 0
4
votes
5
replies
594
views
how to design a guide RNA
genomics
updated 4 days ago by
rfran010
▴ 140 • written 17 days ago by
Bioinfo
• 0
4
votes
3
replies
607
views
Precision-recall curve to compare metagenome classifiers to a gold standard - Is this even a viable method?
classification
recall
precision
metagenome
updated 5 days ago by
sneha.d
• 0 • written 10 months ago by
Bertalan_Takacs
▴ 90
4
votes
12
replies
1.1k
views
Forum:
publicly available data
arrayexpress
GEO
SRA
updated 1 day ago by
Ram
39k • written 3.7 years ago by
Konstantinos Yeles
▴ 110
4
votes
1
reply
976
views
News:
Bioinformatics Workflows with Nextflow
Netflow
reproducibility
Workflows
updated 1 hour ago by
Ram
39k • written 3.5 years ago by
carlopecoraro2
★ 2.3k
4
votes
2
replies
177
views
How to calculate kinship matrix table from vcf file
variants
haplotyping
kinship
heatmap
updated 5 days ago by
chrchang523
10k • written 5 days ago by
rj.rezwan
• 0
4
votes
8
replies
1.6k
views
How to extract promoter sequences from a plant draft genome?
promoter
genome
updated 3 days ago by
Ram
39k • written 3.7 years ago by
Kumar
▴ 100
4
votes
0
replies
767
views
Forum:
Help make UMI-tools even better - take our survey
Survey
UMI
UMI-Tools
updated 23 hours ago by
Ram
39k • written 3.6 years ago by
i.sudbery
17k
4
votes
6
replies
501
views
Help with running ATAC using Encode pipeline
encode
ATAC-seq
6 hours ago by
Chris
▴ 100
4
votes
6
replies
2.4k
views
Forum:
NGS Data Storage Best Practices (Clinical)
NGS
clinical
storage
updated 2 hours ago by
Ram
39k • written 3.5 years ago by
Robert Sicko
▴ 630
4
votes
5
replies
322
views
calculate p value and associated z score for snp-gene pair
snp
association
gene
pvalue
updated 1 day ago by
LChart
2.6k • written 4 days ago by
rheab1230
▴ 140
4
votes
7
replies
3.0k
views
How many storage needs for Whole genome sequencing?
Whole-genome-sequencing
sequencing
updated 6 days ago by
Ram
39k • written 4.0 years ago by
star
▴ 340
4
votes
8
replies
756
views
VEP tab/vcf - Different output
VEP
ensembl
updated 6 hours ago by
Ben_Ensembl
★ 2.2k • written 14 months ago by
Filago
▴ 90
4
votes
12
replies
840
views
Separating text from one column in R
R
updated 5 days ago by
Ram
39k • written 4.0 years ago by
e.jabbari
• 0
4
votes
3
replies
725
views
Forum:
When to ask for rerun from vendors
ngs-vendor
updated 3 days ago by
Ram
39k • written 3.7 years ago by
microfuge
★ 1.9k
4
votes
3
replies
302
views
What does canonical transcript mean in the context of VEP
vep
updated 3 days ago by
Vincent Laufer
★ 2.9k • written 4 days ago by
curious
▴ 720
4
votes
3
replies
726
views
What is the minimum number/threshold of gaps (NNNNNN) permitted in a draft genome?
Assembly
genome
next-gen-sequencing
updated 5 days ago by
Ram
39k • written 3.9 years ago by
Kumar
▴ 100
4
votes
0
replies
1.2k
views
Job:
Ensembl Outreach Officer
training
ensembl
updated 5 days ago by
Ram
39k • written 4.0 years ago by
Emily
23k
4
votes
4
replies
1.4k
views
Forum:
When will the hg19/grch37 finally become obsolete?
Reference-Genome
updated 6 days ago by
Ram
39k • written 4.0 years ago by
gdaly9000
▴ 10
4
votes
6
replies
310
views
Single Cell Rna Seq Using BD Rhapsody
Rhapsody
BD
updated 5 days ago by
Ram
39k • written 5 days ago by
abbas.waseem.gcu
▴ 20
750 results • Page
2 of 15
Recent Votes
Calculating read abundances across MAGs (question)
Comment: Contigs to chromosomes annotation
Comment: Contigs to chromosomes annotation
Comment: Same GEO Accession, different SRR number, how to download this RNA-seq paired-en
Comment: Same GEO Accession, different SRR number, how to download this RNA-seq paired-en
Answer: how to choose an efficient filtering threshold to remove shorter and low quality
Contigs to chromosomes annotation
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Recent Replies
Comment: Contigs to chromosomes annotation
by
GenoMax
129k
I would still recommend using `minimap2` and aligning against reference. It should go pretty fast. You can either work with PAF (default) f…
Comment: Diff Bind Questions
by
Ram
39k
I've moved this to a comment as it does not directly answer OP's question.
Comment: Diff Bind Questions
by
Daniel
▴ 30
I'm very new myself and there's plenty of people who can answer your question better than I can, but here is a resource I found extremely h…
Comment: Contigs to chromosomes annotation
by
alexandru.bologa.marian
▴ 50
If the number of contigs was so small I would manually check each alignment and edit the header of each contig,inserting the corresponding …
Comment: Gviz Coverage Plots
by
Ram
39k
Do not post on multiple fora just because you want a fast response, it's plain rude. At least point to the other post so we know you're ask…
Comment: Limma returned only positive logFC values
by
melissachua90
▴ 40
No the library sizes across conditions should be relatively homogenous because it's from the same dataset. I clustered the samples into sub…
Comment: Limma returned only positive logFC values
by
LChart
2.6k
It shouldn't, unless there's a misspecification in design. Is it the case that the library sizes are very different between the conditions …
Comment: Contigs to chromosomes annotation
by
Darked89
4.3k
For a pure contig to Dmel chromosome BLAST should be OK. I am fan of LAST because it is fairly easy to convert MAF to SAM/BAM and then vi…
Comment: Contigs to chromosomes annotation
by
GenoMax
129k
How many contigs do you have? If the contigs are ~2x number of Drosophila chromosomes (meaning you have long/large contigs) then using a lo…
Comment: Contigs to chromosomes annotation
by
alexandru.bologa.marian
▴ 50
Thank you for your answer! It would be wrong just to BLAST all the contigs from the draft assembly against each reference chromosome of D.…
Comment: Limma returned only positive logFC values
by
melissachua90
▴ 40
Several hundred to 10000 DEGs. Would normalization affect logFC?
Answer: Contigs to chromosomes annotation
by
Darked89
4.3k
Not sure if it is the easiest, but you can map your new assembly to i.e. Dmel genome using LAST: * www: https://gitlab.com/mcfrith/last …
Answer: Gene prediction software
by
Darked89
4.3k
How complete/polished is your catfish genome assembly? Also: do you have some good quality RNA-Seq? With a draft genome it would be…
Comment: Limma returned only positive logFC values
by
LChart
2.6k
It'd be helpful to know how many differentially expressed genes there are. If you've got a handful and they're all upregulated, I wouldn't …
Comment: variant allelic fraction
by
Ram
39k
Cross-posted on bioinfo SE: https://bioinformatics.stackexchange.com/questions/21118/how-to-calculate-the-variant-allelic-fraction-vaf OP,…
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