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1,000 results • Page
1 of 20
Sort: Votes
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Views
Votes
Replies
23
votes
22
replies
40k
views
6 follow
Converting VCF to PLINK .bed binary fileset to check for pedigree errors with KING: How do conversion tools make the PLINK .fam file, without asking …
plink
vcf
fam
gatk
vcftools
updated 6 months ago by
Nicole
• 0 • written 5.1 years ago by
gaelgarcia
▴ 250
22
votes
20
replies
2.1k
views
what is the prefered strategy to treat with blast-less transcriptomes from RNA-seq
blast
RNA-Seq
genome
gene
updated 9 weeks ago by
Ram
39k • written 6.9 years ago by
Farbod
★ 3.4k
20
votes
15
replies
26k
views
8 follow
Converting SNP from chr:pos to rs number using PLINK?
plink
SNP
updated 10 months ago by
Ram
39k • written 7.4 years ago by
dam4l
▴ 190
18
votes
19
replies
1.7k
views
6 follow
Extremely important marker gene has many reads based on IGV viewer but no quantified reads
rna-seq
sequencing
igv
alignment
next-gen
updated 6 months ago by
Ram
39k • written 4.4 years ago by
rbkh09
• 0
18
votes
7
replies
910
views
How to calculate if statistically a variable of a bulk RNA-seq affects the comparison of interest?
DESeq2
Variable
RNA-seq
8 months ago by
Rafael Soler
★ 1.2k
18
votes
4
replies
8.2k
views
How To Find Rna-Seq Data Of Published Papers?
geo
next-gen
RNA-seq
updated 3 months ago by
Ram
39k • written 9.8 years ago by
user
▴ 930
16
votes
8
replies
1.7k
views
8 follow
What are the most important unresolved problems in Bioinformatics?
bioinformatics
updated 8 weeks ago by
Ram
39k • written 6.7 years ago by
chen
★ 2.4k
14
votes
5
replies
2.8k
views
bioinformatics basic training
genome
updated 12 weeks ago by
Ram
39k • written 8.5 years ago by
f.muoghalu
• 0
12
votes
4
replies
505
views
Annotating TSS: By Transcript or by Gene? Code Validation Help Needed!
genome
bed
transcript
TSS
25 days ago by
Rafael Soler
★ 1.2k
12
votes
8
replies
705
views
Align 16S sequence to a reference
16S
sequence
alignment
updated 8 months ago by
Matthias Zepper
3.7k • written 9 months ago by
A_heath
▴ 140
12
votes
13
replies
2.2k
views
Gene Expression and Systems Biology (homework)
gene
homework
updated 6 months ago by
Ram
39k • written 7.9 years ago by
sarathkurichiyil
• 0
11
votes
9
replies
2.1k
views
samtools piping with awk/ bash commands -> Wonky things happen!!!
bash
samtools
awk
updated 5 months ago by
Ram
39k • written 8.0 years ago by
QVINTVS_FABIVS_MAXIMVS
★ 2.5k
10
votes
5
replies
6.5k
views
how to remove asterisk characters from a translated sequences (fasta format)?
sequencing
Assembly
alignment
updated 10 months ago by
Ram
39k • written 7.8 years ago by
seta
★ 1.8k
10
votes
1
reply
3.3k
views
RNA-SeQC, EVER-seq, RSeQC and CollectRnaSeqMetrics, which to use and *why*?
RNA-Seq
qc
updated 10 months ago by
Ram
39k • written 8.0 years ago by
Niek De Klein
★ 2.6k
10
votes
8
replies
1.9k
views
Blast scores...two annotations for the same piece of sequence
alignment
updated 11 months ago by
Ram
39k • written 8.2 years ago by
friasoler
▴ 30
10
votes
14
replies
3.8k
views
ATAC-seq data and deepTools: Small detail with impact on output
bigwig
read-length
deeptools
ATAC-seq
updated 2 days ago by
Ram
39k • written 3.3 years ago by
gable_works
▴ 50
10
votes
15
replies
5.3k
views
convert fasta/gb to vcf
fasta
vcf
genbank
gff
updated 11 weeks ago by
Ram
39k • written 4.7 years ago by
marongiu.luigi
▴ 680
10
votes
6
replies
2.6k
views
which language to use for such a bioinformatics web services infrastructure?
web-services
java
updated 11 weeks ago by
Ram
39k • written 8.0 years ago by
lait
▴ 170
9
votes
4
replies
1.9k
views
[Code] Converte fasta/fa files to fastq
perl
fastq
sed
fasta
updated 10 months ago by
Ram
39k • written 7.6 years ago by
Shicheng Guo
★ 9.3k
9
votes
2
replies
399
views
Answer needed urgently
Deep
updated 8 months ago by
Mensur Dlakic
★ 23k • written 8 months ago by
Deepak
• 0
9
votes
1
reply
5.6k
views
Why does MACS2 report multiple records for the same peak region?
ChIP-Seq
macs
macs2
updated 9 months ago by
Ram
39k • written 7.6 years ago by
James Ashmore
★ 3.4k
9
votes
7
replies
863
views
Reference genome location
reference
positions
FASTA
alignment
genome
updated 5 months ago by
barslmn
★ 1.6k • written 5 months ago by
Batel
• 0
9
votes
4
replies
472
views
RNA seq, secreted protein
protein
gene
secreted
updated 5 months ago by
Joe
21k • written 6 months ago by
Rob
▴ 160
9
votes
4
replies
1.5k
views
On which branch in bioinformatics should a cancer researcher focus on ?
cancer
updated 8 weeks ago by
Ram
39k • written 6.8 years ago by
Bilal
▴ 60
9
votes
4
replies
5.3k
views
How to analyse normalized read count?
RNA-Seq
R
updated 5 months ago by
Ram
39k • written 8.0 years ago by
pbio
▴ 150
9
votes
20
replies
3.4k
views
Solve SAM issues flagged by Picard's ValidateSamFile
Picard
SAM
updated 11 weeks ago by
Ram
39k • written 4.8 years ago by
marongiu.luigi
▴ 680
9
votes
9
replies
1.7k
views
Which hg38 file?
reference
hg38
NCBI
updated 10 months ago by
appropiate
▴ 80 • written 10 months ago by
amy__
▴ 50
9
votes
16
replies
3.1k
views
6 follow
covert SAM to full length fasta
fasta
SAM
updated 11 weeks ago by
Ram
39k • written 4.8 years ago by
marongiu.luigi
▴ 680
8
votes
3
replies
649
views
Package installation error using Bioconda
antismash
Bioconda
6 months ago by
A_heath
▴ 140
8
votes
13
replies
908
views
Mapped reads not mapping to a real sequence?
bam
sam
samtools
kallisto
3 months ago by
txema.heredia
▴ 70
8
votes
11
replies
1.4k
views
using STAR instead of HISAT2
STAR
updated 10 months ago by
Ram
39k • written 10 months ago by
Chris
▴ 100
8
votes
9
replies
2.3k
views
6 follow
Big difference in estimated duplicate reads between forward and reverse of paired-end RNA-seq
RNA-Seq
duplication
fastqc
updated 11 months ago by
rohitsatyam102
▴ 690 • written 3.6 years ago by
Eric Lim
★ 2.1k
8
votes
2
replies
6.2k
views
Differential gene expression analysis in Python
python
R
updated 4 months ago by
Ram
39k • written 19 months ago by
Leendert
▴ 30
8
votes
4
replies
1.7k
views
using different tools to identify differential exprssed genes
rna-seq
RNA-Seq
R
updated 8 months ago by
Ram
39k • written 7.8 years ago by
Anushka
▴ 20
8
votes
12
replies
2.7k
views
Use BLAST Command Line Applications to run a folder of many sequences against a database
BLAST
updated 12 weeks ago by
Ram
39k • written 22 months ago by
daver.v
▴ 30
8
votes
5
replies
11k
views
samtools tview symbols
samtools
updated 7 months ago by
Ram
39k • written 7.9 years ago by
biolab
★ 1.4k
8
votes
5
replies
3.2k
views
Is it possible to guess sequencing platform used based on a FASTQ/BAM file?
BAM
FASTQ
updated 5 months ago by
Ram
39k • written 8.0 years ago by
Andrew
▴ 60
8
votes
6
replies
844
views
How to apply bioinformatic in vaccine design?
Vaccine
updated 6 months ago by
Dunois
★ 2.3k • written 6 months ago by
Jean
▴ 50
8
votes
25
replies
2.1k
views
construction of a database
sql
noSQL
neo4j
database
updated 11 weeks ago by
Ram
39k • written 2.1 years ago by
Debut
▴ 20
8
votes
3
replies
5.0k
views
Bioinformatics project for a beginner
projects
updated 10 months ago by
Ram
39k • written 7.5 years ago by
dharshank.1096
▴ 30
8
votes
9
replies
2.6k
views
error in rstudio
csv
matrix
rstudio
updated 8 months ago by
Ram
39k • written 7.8 years ago by
fi1d18
★ 4.2k
7
votes
7
replies
4.4k
views
RNA-Seq time series analysis using a DESeq2 spline approach yields far too many significant genes
splines
DESeq2
time-series
RNA-Seq
updated 10 days ago by
Ram
39k • written 4.4 years ago by
stu111538
▴ 80
7
votes
4
replies
1.3k
views
So many Zeros (read counting)_NGS sequence analysis with R / Bioconductor: RNA-Seq workflow
alignment
RNA-Seq
R
updated 12 weeks ago by
Ram
39k • written 4.9 years ago by
healing80
• 0
7
votes
2
replies
3.1k
views
Counting reads for gene transcripts with overlapping loci
RNA-Seq
gene
R
updated 5 months ago by
Ram
39k • written 8.0 years ago by
Ruet
▴ 70
7
votes
5
replies
3.7k
views
Trinity de novo transcript assembly too many transcripts
RNA-Seq
Assembly
updated 10 months ago by
Ram
39k • written 8.0 years ago by
Mehmet
▴ 800
7
votes
5
replies
2.3k
views
using machine learning regards to ribo-seq data sets
gene-regulatory-network
ribo-seq
machine-learning
updated 8 months ago by
Ram
39k • written 7.8 years ago by
fi1d18
★ 4.2k
7
votes
8
replies
3.2k
views
DEseq2 design matrix with 3 factors
rna-seq
deseq2
Forum
updated 11 months ago by
1769mkc
★ 1.1k • written 3.0 years ago by
kand3e
▴ 60
7
votes
9
replies
876
views
Tools to check the length of isoforms in reference transcript
transcript
histogram
isoform
7 months ago by
Jjbox
▴ 40
7
votes
8
replies
1.7k
views
How can we time a recent gene duplication event using (neutral?) DNA mutations as molecular clock?
molecular-clock
gene-duplication
phylogeny
updated 4 months ago by
Ram
39k • written 8.1 years ago by
xiaofeng.dong12
▴ 20
7
votes
4
replies
1.4k
views
microarray gene datasets
gene
updated 4 months ago by
Ram
39k • written 8.1 years ago by
bioinfo
▴ 60
1,000 results • Page
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Recent Votes
The .vcf format: is there a file format better suited for the era of pangenomics, and what would it be like?
ChatGPT optimized for bioinformatics questions
Trying to use hmmer to search genes over metagenome assembled genomes
Trying to use hmmer to search genes over metagenome assembled genomes
Comment: Why does Ensembl VEP provide HGVSg for some variants and not others?
Comment: Why does Ensembl VEP provide HGVSg for some variants and not others?
Why does Ensembl VEP provide HGVSg for some variants and not others?
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Recent Replies
Comment: The .vcf format: is there a file format better suited for the era of pangenomics
by
Vincent Laufer
★ 3.0k
@ram - this was as bit of a dirty tactic on my part: I stated it in the extreme to provoke disagreement. I agree with you - the irony is, d…
Comment: The .vcf format: is there a file format better suited for the era of pangenomics
by
Ram
39k
> .vcf is the ideal file format for genomic information; no better file format can be conceived whether in the era of singular linear refer…
Comment: GISTIC from ASCAT
by
Ram
39k
You can use pastebin or GitHub gist to paste more lines, maybe you're being restricted because you're a new user. Did GISTIC give you somet…
Comment: Why does Ensembl VEP provide HGVSg for some variants and not others?
by
Jeremy Leipzig
21k
you're right it's an off-by-one-error on my part. thanks
Comment: A question about the raw RNA-seq processing workflow
by
swbarnes2
13k
are files a,b and c all from the same sample? Or are you trying to align three different samples all together?
Comment: multiqc: group samples by population + boxplot ?
by
GenoMax
130k
Tagging: https://www.biostars.org/u/14100/ Rest of this line is required by biostars code.
Comment: Why does Ensembl VEP provide HGVSg for some variants and not others?
by
Vincent Laufer
★ 3.0k
@genomax thank you for clarifying that - end of an era!
Comment: Why does Ensembl VEP provide HGVSg for some variants and not others?
by
GenoMax
130k
FYI: Emily no longer works for/at Ensembl. That is the reason she has taken out `_ensembl` from her profile. https://www.biostars.org/u/23…
Comment: GISTIC from ASCAT
by
Hyper_Odin
▴ 280
Sorry, this is how much I could paste, there is an error in the website while pasting more lines
Comment: GISTIC from ASCAT
by
Hyper_Odin
▴ 280
Hi Ram, there you go Sample Chromosome Start Position End Position Seg.CN metastasis_H021-ARNHGQ0.47_6.segments_final.tx…
Comment: Why does Ensembl VEP provide HGVSg for some variants and not others?
by
Vincent Laufer
★ 3.0k
copy that. also granted your background i expected nothing less :-)
Comment: Why does Ensembl VEP provide HGVSg for some variants and not others?
by
Vincent Laufer
★ 3.0k
3 quick questions: 1) are you working with a single sample or multisample VCF? 2) what genomic build? (ill assume GRCh38.p14) 3) do you…
Comment: Why does Ensembl VEP provide HGVSg for some variants and not others?
by
Jeremy Leipzig
21k
yes this should be a reproducible example using just those two lines and the latest vep and database on GRCh38
Comment: GISTIC from ASCAT
by
Ram
39k
Can you show me the first 30 lines from the segmentation file you're passing as input to GISTIC please?
Comment: Why does Ensembl VEP provide HGVSg for some variants and not others?
by
Vincent Laufer
★ 3.0k
I have a couple thoughts on this - first, though, would like to confirm that you are on GRCh38?
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