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90,329 results • Page
1 of 1807
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1
vote
2
replies
35
views
How do I find the gene name with the allele number from the databases?
rna-seq
1 hour ago by
Rasoulfarzaneh63
• 0
0
votes
1
reply
40
views
How to implement k fold cv after randomForest
k_fold_cv
R
randomForest
updated 1 hour ago by
Mensur Dlakic
★ 10k • written 4 hours ago by
pt.taklifi
▴ 60
4
votes
2
replies
72
views
How to visualize Multiple Sequence Alignment with python ?
python
clustalw
msa
updated 1 hour ago by
Mensur Dlakic
★ 10k • written 7 hours ago by
Junior
• 0
0
votes
0
replies
58
views
Job:
Bioinformatics Laboratory Head, WEHI, Melbourne, Australia
Australia
Job
1 hour ago by
Gordon Smyth
★ 2.5k
0
votes
0
replies
28
views
Quicker way to download gene sequences from NCBI via E-utils
E-utils
NCBI
Gene
Download
Unix
2 hours ago by
lmlukoseviciute
• 0
0
votes
0
replies
25
views
how reduce gene ontology terms from gprofiler2 output
gprofiler2
GO
DEseq
RNA-seq
3 hours ago by
BISEP
• 0
0
votes
0
replies
32
views
Job:
Postdoc Fellow @ New York City: Alternative Splicing
splicing
genomics
rnaseq
3 hours ago by
fanggang
▴ 100
580
votes
155
replies
64k
views
89 follow
News:
The Biostar Handbook. A bioinformatics e-book for beginners.
handbook
tutorial
training
News
updated 1 day ago by
Biostar
10 • written 4.3 years ago by
Istvan Albert
87k
0
votes
3
replies
86
views
Finding how many times a nucleotide appear in the same position
Beginer
Nucleotide
Python
DNA
updated just now by
cpad0112
15k • written 6 hours ago by
ran
• 0
1
vote
2
replies
56
views
Taxonomy assignment of viral RNA
assembly
taxa
metagenomics
3 hours ago by
biobiu
▴ 120
279
votes
54
replies
10k
views
39 follow
Forum:
What Do You Waste Your Time On
bioinformatics
scripting
Forum
updated 5 hours ago by
ponganta
▴ 160 • written 7.9 years ago by
Asaf
8.6k
3
votes
5
replies
138
views
RNAseq data analysis of pooled data
DESeq2
mapping
featurecounts
clustering
RNA-Seq
updated 5 hours ago by
ponganta
▴ 160 • written 12 hours ago by
luffy
• 0
0
votes
0
replies
40
views
Identify sample mix from NGS data
NGS
samplemix
contamination
celllineauthentication
6 hours ago by
Boberoni
• 0
0
votes
0
replies
40
views
CNV-calling single sample
copynumbervariation
cnv
GATK
na12878
7 hours ago by
Boberoni
• 0
0
votes
0
replies
484
views
Is there any Python or other software that can replace the function "networklevel" in R package "bipartite" for calculation?
R
networklevel
8 hours ago by
153348734
• 0
1
vote
1
reply
54
views
GTF file and Transcript ID
transcriptid
rnaseq
gtf
updated 7 hours ago by
GenoMax
99k • written 9 hours ago by
mtavakoli4030
• 0
0
votes
0
replies
27
views
Couldnot access BSRD database
database
website
BSRD
9 hours ago by
madhujamano
• 0
0
votes
0
replies
36
views
CPM or TPM values as discretization method input
RNA-Seq
discretization
TPM
CPM
6 hours ago by
antmantras
• 0
2
votes
1
reply
59
views
How to extract all columns of CSQ using split-vep plugin of bcftools?
plugin
samtools
bcftools
vcf
split-vep
updated 7 hours ago by
Pierre Lindenbaum
135k • written 10 hours ago by
dare_devil
★ 1.4k
1
vote
2
replies
116
views
Expression of gene of interest across conditions in single-cell data
singlecell
scater
tpm
seurat
Rna-seq
8 hours ago by
kz
• 0
0
votes
1
reply
99
views
bbmap, mapq and uniquelly mapped reads filtering
alignment
mapq
updated 16 hours ago by
GenoMax
99k • written 21 hours ago by
boczniak767
▴ 740
0
votes
2
replies
146
views
Cell composition in each condition of single cell data
cell
composition
single-cell
scProportionTest
14 hours ago by
paria.alipour
▴ 20
1
vote
2
replies
115
views
Generate a file with SNPs given a WGS dataset
annotation
snp
ngs
10 minutes ago by
iibrams07
• 0
0
votes
0
replies
69
views
Calculate relative position of one range with respect to another
Bioconductor
IRanges
GenomicRanges
R
22 hours ago by
Andrew
• 0
0
votes
5
replies
232
views
Limma experiment design and making contrasts
limma
methylation
450k
18 hours ago by
kra277
• 0
1
vote
3
replies
328
views
Keep values from VCF file into Ensembl VEP annotation
SNP
updated 11 hours ago by
dare_devil
★ 1.4k • written 3 months ago by
brunobsouzaa
▴ 520
4
votes
6
replies
231
views
Using outgroup in gene family dendograms
mega
dendograms
1 hour ago by
Rogerio Ribeiro
▴ 50
0
votes
0
replies
77
views
I can not get fasta file with the hit sequences running barrnap
barrnap
bed
updated 22 hours ago by
Ram
32k • written 1 day ago by
pavelasquezv
▴ 10
0
votes
1
reply
80
views
Raw read processing using trimmomatic
trimmomatic
updated 21 hours ago by
boczniak767
▴ 740 • written 1 day ago by
CHINMAYA
• 0
8
votes
8
replies
266
views
How to convert Transcripts ID of rhesus monkey to Transcripts ID of homo sapiens
transcript
rna-seq
updated 7 hours ago by
GenoMax
99k • written 1 day ago by
Quanyou
• 0
0
votes
2
replies
147
views
MASURCA error for multiple entries
masurca
1 day ago by
kilcdincer
• 0
2
votes
3
replies
118
views
How to extract only the specific fasta sequences by matching the ID's to a different source files ?
RNA
alignment
DNA
updated 50 minutes ago by
Prakash
★ 2.1k • written 1 day ago by
pinn
▴ 90
2
votes
2
replies
86
views
Download discontinued gene record from NCBI via E-utils
E-utils
NCBI
Discondinued
Gene
7 hours ago by
lmlukoseviciute
• 0
4
votes
6
replies
232
views
Creating reference genome for mapping and then selecting
mm10
hg38
STAR
RNA-seq
updated 22 hours ago by
Istvan Albert
87k • written 1 day ago by
Dataminer
★ 2.7k
0
votes
2
replies
160
views
ExomeDepth negative BF (bayesian factor) values meaning
WES
DNA-seq
CNV
updated 1 day ago by
German.M.Demidov
★ 2.0k • written 9 weeks ago by
John
▴ 160
2
votes
1
reply
74
views
Tool to find chromosome specific repeats
FISH
repeats
transposons
genomics
updated 1 day ago by
Michael Dondrup
48k • written 1 day ago by
giova34
• 0
0
votes
1
reply
66
views
Different results in limma if group is removed
limma
edgeR
updated 1 day ago by
Kevin Blighe
72k • written 1 day ago by
Palgrave
▴ 20
0
votes
0
replies
34
views
LOOCV on limma results
loocv
limma
cross-validation
updated 1 day ago by
ATpoint
47k • written 1 day ago by
Palgrave
▴ 20
0
votes
1
reply
61
views
About combining the forward and reverse sequence
16srRNA
geneious
updated 1 day ago by
Istvan Albert
87k • written 1 day ago by
ruddhida
• 0
0
votes
0
replies
35
views
mtDNA variant calling
variant
seq
mtdna
fasta
1 day ago by
here_for_learning
• 0
0
votes
1
reply
93
views
How can I revert back the ensemble vep annotated positions to vcf positions?
VCF
ensembl
VEP
updated 1 day ago by
finswimmer
14k • written 1 day ago by
dare_devil
★ 1.4k
0
votes
0
replies
62
views
Pooling normal data in Mutect2
mutect2
pooling
normal
samples
panelofnormals
1 day ago by
Michelle
• 0
0
votes
3
replies
199
views
How do I compare degree and betweenness centrality for different PPI networks?
PPI
centrality
degree
Cytoscape
network
updated 22 hours ago by
Istvan Albert
87k • written 2 days ago by
gemmalouisebaldock
▴ 10
0
votes
1
reply
97
views
What Coverage allele-fraction threshold to use?
snps
somatic
allele-fraction
variants
updated 1 day ago by
German.M.Demidov
★ 2.0k • written 1 day ago by
kristina.mahan
▴ 130
0
votes
1
reply
109
views
Extracting transcripts from whole-transcriptome libraries
galaxy
vcf
rna-seq
updated 1 day ago by
GenoMax
99k • written 1 day ago by
julianneradford
• 0
1
vote
3
replies
149
views
Prokka only creates .log file
miniconda
prokka
ubuntu
bioconda
44 minutes ago by
Camila Martínez
• 0
0
votes
0
replies
137
views
News:
Bioinformatics Open Source Conference 2021
OBF
BOSC
Conference
1 day ago by
Chris Fields
★ 2.2k
4
votes
3
replies
122
views
Hierarchical Clustering of GO terms
Clustering
GO
similarity
Ontology
updated 1 day ago by
Kevin Blighe
72k • written 2 days ago by
The
▴ 160
5
votes
6
replies
972
views
6 follow
correct way of analyzing cell proportions in singlecell data
single-cell RNaseq
updated 1 day ago by
jared.andrews07
9.2k • written 7 months ago by
demoraesdiogo2017
▴ 40
0
votes
1
reply
90
views
TMM normalization for data across two sequencing batches
tmm
normalization
rnaseq
updated 1 day ago by
ATpoint
47k • written 1 day ago by
wiscoyogi
▴ 20
90,329 results • Page
1 of 1807
Recent Votes
Answer: Generate a file with SNPs given a WGS dataset
Comment: How do I find the gene name with the allele number from the databases?
Answer: How to visualize Multiple Sequence Alignment with python ?
C: What Are The Most Common Stupid Mistakes In Bioinformatics?
Comment: Prokka only creates .log file
Answer: How to visualize Multiple Sequence Alignment with python ?
A: Trimmomatic job script to run on multiple pair end read file
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Recent Replies
Comment: Generate a file with SNPs given a WGS dataset
by
iibrams07
• 0
@Dave Carlson. Many thanks. Once at step 6., what should I do to collect only the SNPs and discard other variants ? I need to pipe this col…
Comment: Prokka only creates .log file
by
Camila Martínez
• 0
Thank you! Turns out I need to update a package. I tried creating a new environment just for prokka and everything worked perfectly. Thank …
Comment: How to extract only the specific fasta sequences by matching the ID's to a diff
by
Prakash
★ 2.1k
If you jsut want to extract the sequence based on Id, I not sure if you have one fasta file or multiple fasta file. you can concateante all…
Answer: How do I find the gene name with the allele number from the databases?
by
Rasoulfarzaneh63
• 0
X_84670461 ID chr- SNP position 26_23089878 How do I find the gene name with the allele number from the databases?
Answer: How to implement k fold cv after randomForest
by
Mensur Dlakic
★ 10k
Your setup has what is known as [**the curse of dimensionality**][1] where the number of measured features is much greater than the overall…
Comment: How do I find the gene name with the allele number from the databases?
by
GenoMax
99k
Provide examples whenever any sort of identifiers are being mentioned. Without that information there is no way to answer this question.
Answer: How to visualize Multiple Sequence Alignment with python ?
by
GenoMax
99k
You should also be able to import the alignment into [MEGA][1] for display. [1]: https://www.megasoftware.net/
Answer: How to visualize Multiple Sequence Alignment with python ?
by
Mensur Dlakic
★ 10k
Can't think of a particularly good alignment viewer in python. If you are more interested in result rather than doing it in python, there …
Comment: Using outgroup in gene family dendograms
by
Mensur Dlakic
★ 10k
> Wouldn't a gene that isn't an ABC superfamily member from some distant species suffice as an outgroup candidate here? Most definitely no…
Comment: Testing independence between 5' and 3' terminal sequences in a DNA database
by
Istvan Albert
87k
with that definition I would suspect that all of your sequences are "dependent", I would expect every functional DNA/RNA region to capture …
Comment: Taxonomy assignment of viral RNA
by
biobiu
▴ 120
Thanks! As for the blast option- (1) so do you suggest to just blast the contig against a db of viral RNAs? and (2) is there a comprehensiv…
Comment: Finding how many times a nucleotide appear in the same position
by
cpad0112
15k
#!/usr/bin/env python3 sequences = ["GAGGTAAACTCTG", "TCCGTAAGTTTTC", "CAGGTTGGAACTC", "ACAGTCAGTTCAC", "TAGGTCATTACAG", "TAGG…
Comment: Testing independence between 5' and 3' terminal sequences in a DNA database
by
Anand Rao
▴ 350
Thanks for your reply. Yes, I think I could have explained my problem much better, but rather than change my original post, I will add some…
Answer: Finding how many times a nucleotide appear in the same position
by
Dunois
▴ 610
Here's a little `python` function you can work off of: def count_quer_at_pos_in_seq(seqs, quer = "A"): #Initialize a list…
Comment: Using outgroup in gene family dendograms
by
Rogerio Ribeiro
▴ 50
Thank for the fast reponse. The ABC family is not the best example for this question indeed. The objective of my work is to find genes resp…
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