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121,991 results • Page
260 of 2440
Sort: Rank
Rank
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Votes
Replies
3
votes
0
replies
1.3k
views
Herald:
The Biostar Herald for Thursday, May 11, 2023
herald
2.4 years ago by
Biostar
3.6k
0
votes
4
replies
1.5k
views
csv to custom manifest file
illumina
2.4 years ago by
bioguy24
▴ 230
13
votes
14
replies
4.2k
views
Pan genome based assembly
denovo
ngs
updated 2.3 years ago by
LauferVA
4.8k • written 2.4 years ago by
bioinfo223
▴ 10
6
votes
2
replies
1.2k
views
Why is RNA-Seq library size not constant among samples?
RNA-Seq
sequency_depth
sequencer
library_size
multiplexing
updated 2.4 years ago by
GenoMax
154k • written 2.4 years ago by
FedeXandeR
▴ 20
3
votes
2
replies
1.4k
views
Is the gene-specific PCR efficiency a serious concern for intrasample comparisons in RNA-Seq?
RNA-Seq
normalization
bias
PCR_efficiency
intrasample_comparison
updated 2.4 years ago by
benformatics
4.2k • written 2.4 years ago by
FedeXandeR
▴ 20
0
votes
0
replies
581
views
Create bed file where each column is the number of intersections with another bed file
bedtools
updated 2.3 years ago by
Ram
45k • written 2.4 years ago by
rxs1018
• 0
4
votes
3
replies
2.4k
views
Ncbi protein id mapping to uniprot id
Proteomics
2.4 years ago by
samueldelacamara
• 0
0
votes
0
replies
536
views
XCMS library not centroid mode
xcms
R
2.4 years ago by
t.ru
▴ 20
6
votes
6
replies
8.0k
views
6 follow
How To Retrieve Data From Jgi Automatically Given A Set Of Ids?
r
python
api
xml
updated 2.4 years ago by
GenoMax
154k • written 11.9 years ago by
Manu Prestat
4.1k
1
vote
4
replies
6.7k
views
active.ident slot present but not recognized in seurat object
Seurat
Idents
updated 2.4 years ago by
jv
★ 1.9k • written 2.4 years ago by
e.g.bjornsen
• 0
0
votes
4
replies
1.1k
views
Detect mutations in clonally propagated plants
mutations
Illumina
clonal-propagation
variant-calling
2.4 years ago by
RvV
▴ 30
0
votes
0
replies
493
views
PheWAS - risk/effect allele
GWAS
PheWAS
Open_Targets_Genetics
2.4 years ago by
MH85
▴ 20
3
votes
9
replies
3.8k
views
Finding TF motifs enriched in series of ATAC-seq peaks (using fimo?)
MEME
ATAC-Seq
TF
FIMO
motif
2.4 years ago by
octopuslegs11
▴ 10
2
votes
1
reply
847
views
'Seurat' package
Seurat
R
updated 2.4 years ago by
Ram
45k • written 2.4 years ago by
sooni
▴ 20
0
votes
1
reply
1.3k
views
How can I create more accurate admixture plot like this?
admixture
vcf
plink
updated 2.4 years ago by
Ram
45k • written 2.4 years ago by
kgwkk2
• 0
3
votes
3
replies
2.1k
views
News:
NCBI's IgBLAST version 1.21.0 is now available
IgBLAST
BLAST
T-Cell
NCBI
receptors
2.4 years ago by
PeterC_NCBI
▴ 520
1
vote
2
replies
983
views
`MOFAobject@expectations` is empty list
MOFA2
updated 2.4 years ago by
Ram
45k • written 2.4 years ago by
Dan
▴ 180
1
vote
5
replies
1.8k
views
How to get uniprot accessions from a multi protein sequence fasta file
uniprotkb
uniprot
proteomics
updated 2.4 years ago by
GenoMax
154k • written 2.4 years ago by
Lucas R.F.
▴ 20
5
votes
5
replies
1.5k
views
Normalizing RNA read counts for each gene?
normalization
RNA-seq
metatranscriptomes
updated 2.4 years ago by
Trivas
★ 1.9k • written 2.4 years ago by
pearl2070
▴ 10
8
votes
6
replies
2.2k
views
No differentially expressed genes after multiple testing correction in mice
edgeR
DESeq2
Limma
mouse
RNA-seq
updated 2.4 years ago by
seidel
11k • written 2.4 years ago by
Sara
▴ 40
0
votes
5
replies
2.1k
views
How to trim reads for Chip Seq analysis
base
content
sequence
updated 2.4 years ago by
jkim
▴ 220 • written 2.4 years ago by
users2023
• 0
0
votes
2
replies
802
views
How to use trimmomatic to cut the final part of bases
BASE
SEQUENCE
CONTENT
updated 2.4 years ago by
Ram
45k • written 2.4 years ago by
users2023
• 0
0
votes
1
reply
815
views
Can I perform ANOVA test on rlog data of RNA sequencing counts?
rlog
ANOVA
updated 2.4 years ago by
andres.firrincieli
3.9k • written 2.4 years ago by
Amr
▴ 180
3
votes
1
reply
1.3k
views
How do I use the new human pangenome reference to discover SNV and SV.
pangenome
reference
graph
vg
2.4 years ago by
Pierre Lindenbaum
166k
3
votes
4
replies
1.6k
views
remote tblastn database name(s)
blast
database
tblastn
updated 2.4 years ago by
Mensur Dlakic
★ 30k • written 2.4 years ago by
timothy.kirkwood
▴ 140
0
votes
0
replies
1.3k
views
Understanding the output from Eggnog mapper
inparanoid
orthology
eggnog
2.4 years ago by
The
▴ 180
1
vote
2
replies
1.2k
views
What is the best aligner for stranded RNASeq
aligner
stranded
RNAseq
updated 2.4 years ago by
rpolicastro
13k • written 2.4 years ago by
tarek.mohamed
▴ 370
0
votes
4
replies
1.1k
views
To match fragments within range - Python or awk
awk
python
2.4 years ago by
L_bioinfo
• 0
0
votes
2
replies
1.7k
views
manually calculate log2 fold change and compare
edgeR
log2foldchange
RNA-seq
updated 2.4 years ago by
ATpoint
89k • written 2.4 years ago by
Lea
• 0
1
vote
4
replies
1.2k
views
My VCF file structure is strange and less compatible to data processing programs.
VCF
GATK
SNPs
updated 2.4 years ago by
Istvan Albert
103k • written 2.4 years ago by
kgwkk2
• 0
3
votes
4
replies
3.5k
views
Sub-sampling a BAM to a fixed number of reads
samtools
BAM
updated 2.3 years ago by
Ram
45k • written 2.4 years ago by
matt81rd
▴ 10
0
votes
6
replies
4.8k
views
terminal can't activate base automatically (conda)
conda
updated 4 months ago by
tllee
• 0 • written 4.1 years ago by
Binghong
▴ 20
0
votes
1
reply
691
views
How to analyse scaffold assembly errors?
Scaffold
updated 2.4 years ago by
Istvan Albert
103k • written 2.4 years ago by
xxx_xr
• 0
1
vote
2
replies
919
views
Similarity search and strand difference
blat
bwa-mem2
2.4 years ago by
L_bioinfo
• 0
8
votes
6
replies
3.7k
views
DESeq2 error while using apeglm - optimHess
optimHess
Apeglm
DESeq2
updated 2.4 years ago by
ATpoint
89k • written 2.5 years ago by
vatsay
▴ 40
2
votes
1
reply
1.2k
views
Obtention of the binomial transformed count table with edgeR
RNA-Seq
counts
edgeR
CPM
DeSeq2
updated 2.4 years ago by
ATpoint
89k • written 2.4 years ago by
sofiablancoglez
• 0
0
votes
0
replies
604
views
News:
course- Population genomic inference from low-coverage whole-genome sequencing data
Whole-Genome-Sequencing
Population-Genomics
updated 2.4 years ago by
Ram
45k • written 2.4 years ago by
Physalia-courses
★ 2.6k
1
vote
2
replies
4.7k
views
SnpSift: Annotate vcf file using GNOMAD
GNOMAD
SnpEff
SnpSift
updated 2.4 years ago by
Ram
45k • written 4.5 years ago by
bsmith030465
▴ 250
0
votes
0
replies
2.9k
views
from seurat to scanpy data conversion and re-scaling
transctiptome
eurat
scanpy
conversion
spatial
2.4 years ago by
Omics data mining
▴ 260
0
votes
2
replies
1.5k
views
Gene Set Enrichment Analysis
GSEA
Functional-analysis
2.4 years ago by
ahmad
• 0
1
vote
2
replies
1.5k
views
Problem while downloading SRA using aspera links
sra
aspera
fastq
14 months ago by
chatterjeejayeeta100
• 0
0
votes
0
replies
469
views
download dataset of annotated gene and the domains it contains
domains
database
2.4 years ago by
pick
• 0
1
vote
0
replies
502
views
mirdeep2- unable to extract files for mapping -extract_miRNAs: command not found error
miRNA
miRDeep2
miRNAanalysis
2.4 years ago by
Supernova
• 0
0
votes
5
replies
2.0k
views
combine/merge closet variants into one from mutect2
variants
mutect2
merge
gatk
updated 2.4 years ago by
Istvan Albert
103k • written 2.4 years ago by
J.F.Jiang
▴ 930
0
votes
1
reply
962
views
GDC API: Obtain the Objective Power (or Magnification) of a WSI file
GDC
WSI
TCGA
updated 2.4 years ago by
Zhenyu Zhang
★ 1.3k • written 2.5 years ago by
Martim
• 0
1
vote
5
replies
3.3k
views
What statistical test to apply for DE after CibersortX deconvolution
cibersortx
differential-expression
t-test
deconvolution
2.1 years ago by
Aspire
▴ 390
13
votes
22
replies
5.7k
views
Help with error in GATK variant calling
GATK
updated 2.4 years ago by
Ram
45k • written 2.4 years ago by
Chris
▴ 360
0
votes
5
replies
2.3k
views
Problem with the output of Deeptools PlotProfile: a strange pattern of repetitive summits
deeptools
plotprofile
ChIP-seq
updated 2.4 years ago by
Steven
• 0 • written 3.4 years ago by
Alireza
• 0
1
vote
3
replies
1.4k
views
GRange: Average Metadata Value from 3 Replicates
rtracklayer
GenomicRanges
GRange
2.4 years ago by
RelativeOptics
▴ 40
1
vote
1
reply
1.6k
views
Prefecth-orig and fasterq-dump not working when downloading SRA files (v3.0.5)
Windows
SRAtoolkit
sra
updated 2.4 years ago by
Ram
45k • written 2.4 years ago by
cpaguay
• 0
121,991 results • Page
260 of 2440
Recent Votes
A: Trimmomatic Error: Unable to detect quality encoding
A: Trimmomatic Error: Unable to detect quality encoding
Answer: Nextflow MultiQC runs multiple times due to FASTQC zip name collisions
Comment: Tools to simulate Illumina short read sequences and ONT long reads with a refere
Answer: Nextflow MultiQC runs multiple times due to FASTQC zip name collisions
Answer: Nextflow MultiQC runs multiple times due to FASTQC zip name collisions
Answer: TMM-Normalization
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My personal preference is using [clair3][1]. I'm unsure if CLC didn't work because your compute resources are too limited, or if there are …
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Hi, Wanted to update here that full transcriptome annotations for thousands of hiv genomes (including NL4-3) are now available at https://…
Answer: HIV NL4-3 transcriptome fasta
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You can get full transcriptome annotation for the NL4-3 genomes: https://ccb.jhu.edu/HIV_Atlas/11676/AF324493.2 . Note the accession ID tho…
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The post looks much better now, so you did something. The preview here works fine. It simply can't be that the preview for your original po…
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154k
Black box software has its cons but in instances like what OP needs that may be the only viable option. Their use limits reproducibility as…
Comment: downloading raw bam files from pacbio sequencer
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154k
Have you checked : https://www.pacb.com/connect/datasets/
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No, but a modified version of TMM does: “GeTMM.” See the paper [here](https://bmcbioinformatics.biomedcentral.com/articles/10.1186/s12859-0…
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strayeroliver
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Responding to your answer. - I spent a lot of time formatting it just right, using the ``` methodology you mentioned. It looks very good o…
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by
Phil Ewels
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Found the docs: https://www.nextflow.io/docs/latest/process.html#multiple-input-files | Arity | Name pattern | Staged file names | |---|--…
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jared.andrews07
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No more than running it on native Linux (as that's what WSL is at this point).
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The quality of (modern, SUP basecalled, but certainly not fast basecalled) ONT sequences should be fine, especially for bacterial SNP call…
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What is the median length of raw reads and how many do you have? Has the data been basecalled with "high" or "super" accuracy? > I have …
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This question is about simulating reads and not read mapping.
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I have fun memories of month-long discussions with Illumina support about their GenomeStudio methylation module asking them to provide info…
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