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109,148 results • Page
2 of 2183
Sort: Rank
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Views
Votes
Replies
0
votes
0
replies
92
views
Error at phase 4 when running GeMoMa (homology-based annotation)
Homology
GeMoMa
Annotation
Genome
1 day ago by
breannar
• 0
12
votes
9
replies
717
views
6 follow
How to find promoter sequence of a gene?
promoter
1 day ago by
sunyeping
▴ 80
1
vote
4
replies
230
views
bash command to process a line
linux
command
updated 1 day ago by
GenoMax
127k • written 1 day ago by
saadleeshehreen
▴ 110
0
votes
0
replies
88
views
News:
Virtual RAD-seq Analysis Workshop!
workshops
popgen
genomics
rad-seq
1 day ago by
mia.nahom
▴ 10
1
vote
4
replies
185
views
Centromere and telomere positions for Chm13v2 assembly
centromere
chm13v2
1 day ago by
arsala521
▴ 10
0
votes
5
replies
255
views
featureCounts problem in reading Gff
featureCounts
GFF
RNA-seq
updated 1 day ago by
Ram
38k • written 1 day ago by
Beatrice
• 0
4
votes
0
replies
82
views
Tool:
PyComplexHeatmap: a Python package to visualize multimodal genomics data
visualization
Python
ComplexHeatmap
PyComplexHeatmap
updated 1 day ago by
Ram
38k • written 1 day ago by
Wubin
▴ 40
2
votes
2
replies
153
views
Retrieve hgnc_symbol from XM_ refseqs using BiomaRt
refseq_mrna_predicted
biomaRt
refseq
XM
21 hours ago by
ladina.hoesli
• 0
0
votes
1
reply
125
views
Time change in expression vs time change in phenotype
RNA-Seq
DGE
DESeq2
1 day ago by
Ivan
• 0
0
votes
0
replies
79
views
How to perform a gsva assessing for the directonality of the genes.
gsva
1 day ago by
roybatty269
• 0
0
votes
4
replies
910
views
activity of unloaded/unassembled Tn5
sequencing
next-gen
updated 1 day ago by
ATpoint
70k • written 5.1 years ago by
zhaohainancau
• 0
7
votes
7
replies
507
views
Nextflow rnaseq finishing early
RNA-seq
nextflow
updated 1 day ago by
Ram
38k • written 1 day ago by
Raygozak
★ 1.4k
3
votes
6
replies
404
views
ClusterProfiler enrichKEGG – remove organism name in plots?
KEGG
ggplot2
enrichKEGG
ClusterProfiler
updated 1 day ago by
jv
★ 1.0k • written 8 days ago by
Sian
▴ 20
2
votes
0
replies
110
views
Herald:
The Biostar Herald for Tuesday, March 28, 2023
herald
1 day ago by
Biostar
1.6k
1
vote
4
replies
460
views
Retrieve protein sequence from Mgnify given only accession code
Mgnify
API
updated 1 day ago by
biomarco
▴ 20 • written 9 months ago by
jscience
• 0
1
vote
1
reply
202
views
Browsing MGnify IDs and clusters
metagenomics
mgnify
ebi
1 day ago by
biomarco
▴ 20
0
votes
0
replies
77
views
calculation of calibration factors using impuation reference panel and ethnicity
GWAS
Calibration
factor
1 day ago by
parveenkayenat
• 0
1
vote
4
replies
223
views
Artificial reads - remove multiple mapped reads against reference genome, and only keep reads that completely match without any mismatches - samtools
samtools
18 hours ago by
Agamemnon
▴ 60
0
votes
0
replies
79
views
Haploview linkage format .ped and .info file error
plink
Haploview
vcftool
1 day ago by
Nai
▴ 50
6
votes
1
reply
168
views
what is IGV visualization lighter color variants stand for
visualization
vcf
IGV
updated 1 day ago by
Jorge Amigo
14k • written 1 day ago by
zhangfish
▴ 50
0
votes
2
replies
1.6k
views
Error when changing the database for minfi dropLociWithSnps
SNP
minfi
methylationEPIC
illumina
methylation
updated 1 day ago by
Satu
• 0 • written 5.7 years ago by
Ellen O
▴ 20
0
votes
0
replies
115
views
How to export GWAS lists available in Open Targets database
GWAS
gene
openTargets
16 hours ago by
dzisis1986
▴ 60
0
votes
0
replies
113
views
Bcftools consensus generates mismatched consensus sequence
Consensus
sequence
1 day ago by
Duy
• 0
0
votes
0
replies
79
views
Is there a function to get the number of aligned sites between pairs of sequences in a multiple sequence alignment in R?
msa
R
1 day ago by
audrey
• 0
0
votes
0
replies
100
views
Nucleotide substitution model and neighbor-joining tree
phylogeny
substitution
mega
neighbor-joining
modeltest
18 hours ago by
poecile.pal
▴ 50
5
votes
7
replies
374
views
Most efficient way to run Diamond against a very very large database (i.e., NCBI's NR)?
protein
annotation
alignment
diamond
nr
1 day ago by
O.rka
▴ 650
0
votes
0
replies
99
views
Octopus advanced vcf guide: Example of overlapping vcf calls with *
vcf
spanning
alleles
octopus
1 day ago by
penington.j
• 0
0
votes
0
replies
117
views
how can we improve genome assembly levels ? from contig to complete using bioinformatics pipelines?
contig
genome
pipelines
assembly
updated 1 day ago by
Ram
38k • written 1 day ago by
vasudhapai
• 0
3
votes
3
replies
229
views
Editing fasta headers
fasta
updated 1 day ago by
Ram
38k • written 2 days ago by
Zoe
• 0
0
votes
0
replies
124
views
Link products to their genes
RNA-SEQ
GO
edgeR
1 day ago by
Pegasus
▴ 80
0
votes
0
replies
119
views
Trajectory analysis using Monocle3 with Seurat sub-clustering
scRNA-seq
Trajectory
Seurat
analysis
Monocle3
2 days ago by
joonhong kwon
▴ 40
0
votes
0
replies
125
views
News:
The Canadian Bioinformatics Workshops are back for summer 2023
CBW
training
workshop
1 day ago by
bioinformatics.ca
• 0
0
votes
1
reply
172
views
Error parsing strand (?) from GFF line
assembly
updated 1 day ago by
cmdcolin
★ 2.9k • written 2 days ago by
hafiz.talhamalik
▴ 350
0
votes
3
replies
245
views
Sample size for population genetics
Population-genetics
sample-size
updated 2 days ago by
Jeremy Leipzig
21k • written 2 days ago by
zimmer.schweiz
• 0
1
vote
0
replies
137
views
List of Ongoing and Planned Long Read Sequencing studies?
long-read-sequencing
third-generation
updated 2 days ago by
Ram
38k • written 2 days ago by
Vincent Laufer
★ 2.5k
3
votes
8
replies
3.8k
views
counting the unmapped reads
RNA-Seq
updated 2 days ago by
chemkhi.ali13
• 0 • written 7.9 years ago by
fi1d18
★ 4.1k
0
votes
1
reply
159
views
SNP ID (rsID) to Chr no. and Position
Annotation
2 days ago by
Jewahir
• 0
0
votes
0
replies
125
views
how to plot distribution of SNPs across a set of genes based on distance between snp and gene
snp
genes
updated 2 days ago by
Ram
38k • written 2 days ago by
rheab1230
▴ 140
0
votes
0
replies
108
views
Reactome Species Comparison - analysis table
reactome
1 day ago by
a11msp
▴ 120
0
votes
1
reply
202
views
Discordinant aligment
Paired-end
HISAT2
updated 2 days ago by
Istvan Albert
97k • written 2 days ago by
ali
• 0
0
votes
1
reply
153
views
Using multimaping reads or unique reads on featurecounts?
featurecounts
HISAT2
updated 2 days ago by
GenoMax
127k • written 2 days ago by
omargmc.tak
• 0
0
votes
0
replies
118
views
News:
Next-Generation Sequencing Data Analysis: A Practical Introduction (May 3-5, 2023 in Munich, Germany)
NGS
DNA-Seq
calling
RNA-Seq
workshop
variant
2 days ago by
David Langenberger
9.9k
0
votes
1
reply
263
views
module and trait correlation for WGCNA
treatment
WGCNA
relation
microarray
module-treatment
updated 2 days ago by
andres.firrincieli
3.2k • written 3 days ago by
Shriyansh
• 0
3
votes
7
replies
260
views
1000 genomes hg38 with dbSNP rsid
1000genomes
dbsnp
updated 2 days ago by
Ram
38k • written 2 days ago by
Vince
▴ 150
0
votes
0
replies
98
views
How to import impute2.dosage files to analyse it in R (GWAS)
regression
GWAS
impute2
dosage
2 days ago by
Sebastian
• 0
5
votes
3
replies
425
views
What's the correct way to map to hg38 with alternative contigs?
NGS
bwa
2 days ago by
Belanov
▴ 10
6
votes
4
replies
183
views
Download NCBI compiled protein database for specific genus
protein
NCBI
updated 2 days ago by
GenoMax
127k • written 2 days ago by
saadleeshehreen
▴ 110
0
votes
0
replies
98
views
Michigan Imputation server failed job
michigan-imputation-server
vcf
updated 2 days ago by
Ram
38k • written 2 days ago by
Najla
• 0
0
votes
0
replies
97
views
MD simulation error
MD
schrodinger
updated 2 days ago by
Ram
38k • written 2 days ago by
mixmatchey
• 0
0
votes
0
replies
103
views
File has zero value indivuals
Haploview
updated 2 days ago by
Ram
38k • written 2 days ago by
Nai
▴ 50
109,148 results • Page
2 of 2183
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Answer: Variant caller reports a homozygous variant genotype, but more reads are associa
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Comment: GO enrichment analysis
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Answer: Any tips in landing a bioinformatic job?
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Vincent Laufer
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Do you have a public facing github page (or equivalent) that provides examples of bioinformatics workflows you've created? For myself, if …
Comment: Align miRNA library (small RNA-seq) without trimming
by
Paola
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Hi Ming Untrimmed reads have 76bp in average.
Answer: Align miRNA library (small RNA-seq) without trimming
by
Ming Tommy Tang
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bowtie 1 is good for short read < 50bp, how long is your read? bowtie2 is better for reads > 50 bp
Comment: Differences in RNAseq Variant Calling and Allele Specific Expression
by
afei
• 0
Hi! I'm also confused by this. And the site (https://gatkforums.broadinstitute.org/gatk/categories/gatk-support-forum) is closed. Have you …
Comment: Variant caller reports a homozygous variant genotype, but more reads are associa
by
rebeliscu
▴ 50
Indeed, I thought the quality might be a factor. Still, given the information, it seems odd to me that that call was made. Thanks for you…
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▴ 730
To generate a VCF file one would normally pipe the input of an `mpileup` command into an actual `call` command. For example: ``` bcftools …
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Your assumption is correct - AlphaFold pTM has nothing to do with post-translational modifications. See [**here**][1]. Not to discourage…
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I had this issue today and was able to resolve it by changing the random seed Admixture uses by adding `-s time` (which sets the random see…
Answer: Total No of Genes of GENCODE Release 43
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ahmad
• 0
The following is the correct code gtf_43<-rtracklayer::import('gencode.v43.primary_assembly.annotation.gtf') dtgtf_43<-data.frame(gtf_4…
Comment: Total No of Genes of GENCODE Release 43
by
ahmad
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Hello, thanks for replying, by mistake I paste the wrong code. the following is the corrected gtf_43<-rtracklayer::import('gencode.v43…
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I have no idea what that is besides a bunch of jumbled sequences. You'll need look up the structure of the reads / library from wherever yo…
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First thing: kallisto cannot interface with UMI-tools (kallisto doesn't use read headers and therefore you're stuck with "the kallisto way"…
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There is some somatic SV study on these HCC1395: https://doi.org/10.1186/s13059-022-02816-6. There is also a CNA preprint from years ago b…
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Hmm, not sure why `subset` doesn't match to '0:CD8 T cell' but maybe it's the ":"? An alternative option is the following: ``` idx <- whi…
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