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 year
all time
today
this week
this month
this year
1,000 results • Page
4 of 20
Sort: Rank
Rank
Views
Votes
Replies
0
votes
1
reply
191
views
News:
EMBL-EBI virtual course | Introduction to RNA-seq and functional interpretation
RNA-seq
updated 8 days ago by
Ram
40k • written 8 days ago by
Rebecca
• 0
2
votes
7
replies
663
views
Weirdness in annotation (missing allele frequencies)
allele-frequency
gnomad
annovar
updated 16 hours ago by
Jeremy Leipzig
21k • written 8 days ago by
Can Abdullah
• 0
1
vote
3
replies
243
views
Finding sequences in unannotated genomes using reference coordinates
consensus
VCF
updated 8 days ago by
Ram
40k • written 8 days ago by
Prangan
▴ 20
0
votes
1
reply
220
views
High amount of intronic/intergenic reads in SMARTer stranded total bulk RNAseq
RNA-seq
DNA
SMARTer
updated 8 days ago by
Ram
40k • written 8 days ago by
Mat
▴ 60
2
votes
5
replies
355
views
How to check RNAseq support for annotated genes?
gene
RNA-seq
annotation
updated 4 days ago by
Michael
53k • written 8 days ago by
BioinfoBee
• 0
0
votes
0
replies
350
views
Why dbConnect GEOmetadb_demo.sqlite shows some information while dbConnect GEOmetadb.sqlite shows no information
R
GEO
GEOmetadb
updated 8 days ago by
Pierre Lindenbaum
157k • written 8 days ago by
nonaddldy
▴ 10
1
vote
0
replies
170
views
News:
Online Training - Bioinformatics Pipeline Development with Nextflow (November 15-17, 2023)
nextflow
automation
pipeline
development
8 days ago by
David Langenberger
10k
2
votes
5
replies
379
views
ATAC-seq troubleshoot - Just Noise
ATAC-seq
updated 4 days ago by
ATpoint
77k • written 9 days ago by
vk
▴ 40
2
votes
2
replies
255
views
Simulate short-read RNA-seq data from long-read RNA-seq data
polyester
single-cell
simulation
short-read
long-read
4 days ago by
rhonddaskl
• 0
4
votes
4
replies
434
views
DESeq2 analysis using two featureCounts generated from different studies
RNA-seq
DESeq2
8 days ago by
abedkurdi10
▴ 190
4
votes
4
replies
364
views
Filtering VCF to divide with equal sizes
bcftools
vcf
updated 9 days ago by
Ram
40k • written 9 days ago by
avelarbio46
▴ 30
0
votes
0
replies
175
views
High pvalues when using clusterProfiler for seurat
clusterProfiler
9 days ago by
Ahmed
• 0
5
votes
2
replies
258
views
kallisto normalized TPM values without bootstraps
tpm
cibersort
sleuth
kallisto
RNA-seq
8 days ago by
butterman16
▴ 20
5
votes
7
replies
440
views
Salmon index not progressing
salmon
updated 8 days ago by
Michael
53k • written 9 days ago by
camillab.
▴ 140
0
votes
0
replies
170
views
scanpy problem for empty cells
scanpy
updated 9 days ago by
Ram
40k • written 9 days ago by
Andy
▴ 90
0
votes
0
replies
172
views
Current landscape of approaches to scRNA-seq with nanopore sequencers?
scRNA-seq
nanopore
single-cell
6 days ago by
LauferVA
3.7k
0
votes
1
reply
216
views
How to download genomes and proteins from JGI in bulk via the command line?
jgi
cli
updated 9 days ago by
Ram
40k • written 9 days ago by
O.rka
▴ 680
2
votes
1
reply
223
views
News:
Successful NCBI NIAID Codeathon on VCF Files in SARS-CoV-2 Genomics
NCBI
Codeathon
updated 6 days ago by
chrchang523
10k • written 9 days ago by
PeterC_NCBI
▴ 330
3
votes
4
replies
401
views
Chromosome bias on RNA-Seq differential gene expression analysis
chromosome-bias
RNA-seq
8 days ago by
blz
▴ 30
0
votes
5
replies
465
views
genome data downloads for various strains
gisaid
hass-marr
updated 5 days ago by
Ram
40k • written 9 days ago by
iftikharmaryam123
• 0
0
votes
0
replies
185
views
Illumina methylation EPIC V2 array
ewas
methylation
enrichment
missMethyl
EPIC
9 days ago by
juliviglino
• 0
3
votes
2
replies
333
views
Identifying common DEGs among multiple datasets
R
DEG
updated 9 days ago by
Barry Digby
★ 1.2k • written 10 days ago by
Shma
• 0
4
votes
8
replies
601
views
Assistance with Fungal Genome Annotation Using Maker and BLAST
gff3
fasta
maker
xml
blastp
5 days ago by
Edoardo
• 0
0
votes
0
replies
168
views
News:
Workshop - Single-Cell RNA-Seq Data Analysis: A Practical Introduction (November 8-10, 2023 in Berlin)
workshop
scRNA-Seq
RNA-Seq
single-cell
updated 9 days ago by
Ram
40k • written 9 days ago by
David Langenberger
10k
3
votes
3
replies
368
views
Forum:
Importance of Data Structures for Bioinformatics?
data-structures
updated 9 days ago by
Ram
40k • written 10 days ago by
S
• 0
0
votes
2
replies
285
views
How to find positions with higher depth relative to their surroundings
depth
python
samtools
updated 9 days ago by
xiaoguang
▴ 130 • written 10 days ago by
hyperdx1
• 0
0
votes
0
replies
159
views
News:
Research Breakthrough in Identifying Viral Escape Mutations for Improved Therapeutic Design
sequence-analysis
sars-cov-2
spike-protein
updated 9 days ago by
Ram
40k • written 10 days ago by
Prem
• 0
3
votes
2
replies
276
views
How to retrieve LoF and missense variants in WES data?
bcftools
variants
plink
SNPs
updated 10 days ago by
luffy
▴ 60 • written 10 days ago by
_quantum_girl_
▴ 10
0
votes
0
replies
369
views
Recommended workflow for identifying the genomic location and copy-number of an insert with a known sequence from WGS Nanopore fastq files
Nanopore
WGS
Long-Read
updated 9 days ago by
Ram
40k • written 10 days ago by
dk0319
▴ 70
3
votes
1
reply
198
views
What is the difference between norm --multiallelics -any versus --atomize?
bcftools
updated 10 days ago by
Ram
40k • written 10 days ago by
a615ebfb
▴ 30
4
votes
0
replies
206
views
Herald:
The Biostar Herald for Wednesday, September 20, 2023
herald
10 days ago by
Biostar
2.0k
1
vote
4
replies
322
views
I need to retrieve a set of protein and mRNA sequences
Protein
mRNA
sequences
updated 10 days ago by
Ram
40k • written 10 days ago by
george
• 0
0
votes
1
reply
211
views
Esearch, Epost, and Efetch for Large Datasets in Biopython
eutils
biopython
entrez
updated 9 days ago by
Ram
40k • written 10 days ago by
Salem
• 0
1
vote
2
replies
249
views
GSEA Result Visualization in R
r
enrichplot
gsea
visualization
enrichResult
10 days ago by
Cortney
• 0
1
vote
2
replies
272
views
How to separate proteins on the same chain?
pdb
protein
updated 9 days ago by
Ram
40k • written 10 days ago by
Zayyan
▴ 10
0
votes
2
replies
246
views
how to evaluate SNPs that are regulating same gene expression across multiple tissues
snp
GTEx
updated 10 days ago by
LChart
3.4k • written 10 days ago by
rheab1230
▴ 140
3
votes
10
replies
534
views
STAR index not working
STAR
RNA-Seq
9 days ago by
camillab.
▴ 140
1
vote
2
replies
389
views
How to display all top markers in the heatmap by DoHeatmap (Seurat) when there are duplicates of top marker genes for several cell clusters
DoHeatmap
Seurat
10 days ago by
alwayshope
▴ 30
2
votes
3
replies
294
views
Can I infer the fraction of replicating cells from bulk RNA-seq data?
replication
apoptosis
updated 10 days ago by
Ram
40k • written 10 days ago by
txema.heredia
▴ 80
0
votes
1
reply
173
views
Prank checkpoint and restore?
prank
alignment
updated 10 days ago by
Ram
40k • written 10 days ago by
Pit
• 0
0
votes
0
replies
1.0k
views
Job:
Research Scientist 5 – Bioinformatics and Computer Biology, Center for Dementia Research (CDR), Nathan Kline Institute for Psychiatric Research
Neuroscience
Biostatistics
updated 10 days ago by
Ram
40k • written 10 days ago by
cdrinfo
• 0
0
votes
1
reply
189
views
gffread outputs empty gtf file
gff
gffread
gtf
updated 10 days ago by
inedraylig
▴ 20 • written 10 days ago by
sumitra.20
• 0
0
votes
13
replies
592
views
STAR Intron Motif Script Gives Segmentation fault Error
STAR
Linux
7 days ago by
Y
• 0
5
votes
7
replies
506
views
Elusive syntax error in Snakefile
snakemake
updated 10 days ago by
Ram
40k • written 11 days ago by
Giuseppe Giovanni
▴ 30
1
vote
3
replies
253
views
Sub-sampleing bam files based on sequencing_summary.txt (guppy output)
samtools
guppy
updated 10 days ago by
GenoMax
134k • written 10 days ago by
anika.john
• 0
8
votes
10
replies
746
views
Inflated GWAS test statistic after merging multiple batches of genotype dataset imputed differently
genotype
imputation
gwas
updated 10 days ago by
LauferVA
3.7k • written 11 days ago by
Amy
▴ 20
0
votes
13
replies
706
views
Dealing with transcriptome sequences that are smaller than their respective genes
blastn
Trinity
Transcriptome
RNA-seq-analysis
De-novo-transcriptome-assembly
8 days ago by
langziv
▴ 50
2
votes
2
replies
220
views
Kraken2 recovering only classified reads
Kraken2
taxonomy
classification
10 days ago by
SushiRoll
▴ 110
0
votes
0
replies
121
views
Any way to predict hormone biosynthesis pathways in understudied organisms?
genomics
orthologs
biosynthesis-pathway
updated 10 days ago by
Ram
40k • written 10 days ago by
Mark
• 0
2
votes
4
replies
330
views
Refseq annotation | Populus trichocarpa
R
RNA-seq
plants
Refseq
updated 10 days ago by
Ram
40k • written 10 days ago by
P
• 0
1,000 results • Page
4 of 20
Recent Votes
A: .gstmp extension on .bam files downloaded from google bucket; and EOF marker is
Comment: Significance testing of top vs. random SNPs
Answer: Search RCSB with a list of protein names?
A: running RAxML and MrBayes over concatinated multiple sequence alignments
Comment: Weirdness in annotation (missing allele frequencies)
Comment: Weirdness in annotation (missing allele frequencies)
Comment: ncbi error report log for validate fastq issue
Recent Locations •
All
Japan,
3 minutes ago
United States,
9 minutes ago
United States,
17 minutes ago
Seattle, WA USA,
23 minutes ago
Pakistan,
25 minutes ago
China,
28 minutes ago
India,
38 minutes ago
Recent Awards •
All
Commentator
to
dsull
★ 4.8k
Scholar
to
liorglic
★ 1.3k
Popular Question
to
natasha.sernova
★ 3.9k
Popular Question
to
ntsopoul
▴ 50
Teacher
to
benformatics
3.8k
Popular Question
to
iislam
• 0
Scholar
to
ATpoint
77k
Recent Replies
Comment: Getting the overlap between two GTF files
by
Alex Reynolds
35k
What would that be?
Answer: Encountering Error while Running 'make vcf' in Biostar Handbook
by
Tully
• 0
@ialbert ,I am deeply immersed in the fog and request the help ,please
Comment: bedtools intersect by position & stand not working even with common regions
by
rfran010
▴ 830
are you sure bedtools can handle the non-standard location of strand information?
Answer: Getting the overlap between two GTF files
by
rfran010
▴ 830
Maybe somebody knows something I don't, but I feel like bedtools should be able to handle your gtf files directly. If it's not done alre…
Answer: vcf.gz to vcf
by
Mark
★ 1.3k
As the error says, the file is not compressed. In linux the file extension is essentially optional. The file could be named `my.vcf.txt` ye…
Answer: Search RCSB with a list of protein names?
by
Jiyao Wang
▴ 340
You can use NCBI esearch to search the protein names against the structure database to get the PDB IDs, then retrieve the structures.
Answer: How to get ncol = nrow?
by
Mark
★ 1.3k
Without your actual data, it's hard to assist. I think what you're asking is 'how do I rename the rows of my dataframe(s)'. Taking the …
Comment: MAKER: WARNING: Could not get initialization lock. Trying Again...
by
GenoMax
134k
What kind of hardware are you running this on? You need to have the right kind of hardware (multiple CPU's not just cores), MPI libraries a…
Answer: Getting the overlap between two GTF files
by
Alex Reynolds
35k
Using `bedops --intersect` and `gtf2bed` will get their common genomic space: ``` bedops --intersect <(gtf2bed < transcripts.gtf) <(gtf2be…
Comment: Encountering Error while Running 'make vcf' in Biostar Handbook
by
Tully
• 0
```bash # Obtain the makefile curl -s http://data.biostarhandbook.com/make/snpcall.mk > Makefile # Run the makefile make vcf ``` Error me…
Comment: Encountering Error while Running 'make vcf' in Biostar Handbook
by
Tully
• 0
> System Information: Ubuntu 22.04 (WSL2) > > Shell: zsh > > Installation Verification: Yes, doctor.py OK [1]: https://www.biostarhand…
Comment: Retrieve The Reads And Fastq From Bam File
by
Reem
• 0
Did it affect the bamtofastq output file? if so how did you solve the problem? Thanks
Answer: How to import bigwig files into igvR
by
Trivas
★ 1.5k
You could try seeing if this fixes your issue with rtracklayer: https://support.bioconductor.org/p/p133244/
Comment: Weirdness in annotation (missing allele frequencies)
by
Jeremy Leipzig
21k
0.60625 is 97/160 so if you have 80 individuals in your VCF that's an internal allele frequency, not gnomAD
Comment: Weirdness in annotation (missing allele frequencies)
by
Can Abdullah
• 0
Yes, I was confused as well. I think the same. Maybe Annovar uses some other resources besides gnomad, but it does not make sense. Also, I …
Traffic: 1382 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