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121,967 results • Page
225 of 2440
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0
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566
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UMI count and cell number (scRNA-seq)
scRNA-seq
Cellranger
Seurat
updated 2.2 years ago by
Ram
45k • written 2.2 years ago by
Song
▴ 10
0
votes
3
replies
3.3k
views
AvgExpression error in seurat: invalid name for slot of class “Assay5”: check.matrix
10X-genomics
heatmap
single-cell
updated 2.2 years ago by
Ram
45k • written 2.2 years ago by
AW
▴ 10
1
vote
0
replies
1.1k
views
Job:
A 4 years Ph.D. in Computational Biology in Sweden!
PhD
Elhaik
Israelites
Vikings
Sweden
2.2 years ago by
eranelhaik
▴ 30
5
votes
7
replies
2.7k
views
Speed up vg call ?
vg_team
vg
updated 2.2 years ago by
Maxine
▴ 50 • written 2.8 years ago by
colindaven
8.0k
0
votes
0
replies
677
views
Kraken2 + Bracken with short reads (~20 bases) as input
Bracken
smallRNAseq
Kraken2
2.2 years ago by
jammydodger123456
▴ 40
0
votes
1
reply
584
views
Gene signature into scoring method
geneset-enrichment
rna-seq
r
updated 2.2 years ago by
jared.andrews07
★ 19k • written 2.2 years ago by
sohail.mbio
• 0
10
votes
16
replies
3.1k
views
Filter gene with low count in RNA-seq using a function from edgeR
edgeR
RNA-seq
updated 2.2 years ago by
petebio
▴ 100 • written 2.2 years ago by
Chris
▴ 360
0
votes
3
replies
2.1k
views
Seurat IntegrateData function returning an error
integrateData
seurat
updated 2.2 years ago by
Ram
45k • written 2.2 years ago by
cassy
• 0
1
vote
3
replies
1.1k
views
Estimating own weights in TWAS/FUSION - manual
twas-fusion
twas
updated 2.2 years ago by
Ram
45k • written 2.2 years ago by
Genotepes
▴ 950
0
votes
1
reply
636
views
piRNA seq
piRNA
updated 2.2 years ago by
biofalconch
★ 1.3k • written 2.2 years ago by
daffodil
▴ 10
3
votes
5
replies
1.7k
views
High discordant alignment with HISAT2 Mus musculus
HISAT2
RNA-seq
updated 2.2 years ago by
GenoMax
154k • written 2.2 years ago by
AHerik
▴ 40
2
votes
8
replies
5.1k
views
Separate single cell BAM file by the cell barcode
BAM
scRNAseq
single-cell
updated 10 months ago by
GenoMax
154k • written 2.2 years ago by
zbidav
▴ 30
1
vote
3
replies
1.1k
views
Classification for low quality variant on IGV
bam
igv
updated 2.2 years ago by
dthorbur
★ 3.1k • written 2.2 years ago by
amy__
▴ 250
0
votes
1
reply
705
views
Expanding gVCF box from GATK
GATK
VCF
gVCF
updated 2.2 years ago by
Jeremy Leipzig
23k • written 2.2 years ago by
Axzd
▴ 80
1
vote
7
replies
2.8k
views
cannot execute binary file: Exec format error
linux
updated 2.2 years ago by
Michael
56k • written 2.2 years ago by
applepie
▴ 10
3
votes
2
replies
1.3k
views
Bio.Phylo cut the tree (python)
phylogeny
cuttree
biopython
tree
Bio.Phylo
2.2 years ago by
Fedor
▴ 10
3
votes
5
replies
3.3k
views
Differential Gene Expression analysis in Bulk RNA Seq - using Count Matrix as input
DESeq2
BulkRNASeq
updated 2.0 years ago by
ATpoint
89k • written 2.2 years ago by
applepie
▴ 10
1
vote
2
replies
1.4k
views
Salmon error (ex. transcript id appears in the BAM head, but was not in the provided FASTA file)
Salmon
expression-matrix
Transcript-level
updated 2.2 years ago by
Ram
45k • written 2.2 years ago by
tonyya21
• 0
1
vote
1
reply
1.4k
views
Calculating coverage/depth for nanopore dRNAseq reads with reference transcriptome/genome
rnaseq
coverage
nanopore
updated 2.2 years ago by
biofalconch
★ 1.3k • written 2.2 years ago by
kenneditodd
▴ 50
0
votes
1
reply
887
views
Inferring undisclosed 5mer in proprietary SMARTer oligo sequence
smart-seq
scrnaseq
updated 2.2 years ago by
Pei
▴ 240 • written 2.2 years ago by
kevin.stachelek
▴ 80
1
vote
1
reply
745
views
Multiple sequence aligment orientation
multiple-sequence-alignment
updated 2.2 years ago by
Ram
45k • written 2.2 years ago by
Josselin
▴ 10
0
votes
1
reply
632
views
CIBERSORT, frequency and fraction, immune cell infiltration
CIBERSORT
2.2 years ago by
Rob
▴ 180
0
votes
1
reply
801
views
How can I sort the circular heatmap labels alphabetically in R?
circular-heatmap
circlize
r
circos
2.2 years ago by
logbio
▴ 30
3
votes
6
replies
1.7k
views
plink QC
QC
Plink
2.2 years ago by
karthick
▴ 10
0
votes
10
replies
2.7k
views
Deseq2 questions
deseq2
transcriptome
updated 2.2 years ago by
Asaf
10k • written 2.2 years ago by
UserA
• 0
3
votes
2
replies
1.1k
views
GTF file tomato
tomato
GTF
GFF
updated 2.2 years ago by
GenoMax
154k • written 2.2 years ago by
javadkarimi10
• 0
1
vote
3
replies
1.6k
views
Phasing Classical HLA Alleles
Haplotype
UKBiobank
HLA
Phasing
updated 2.2 years ago by
Ming Tommy Tang
★ 4.7k • written 2.2 years ago by
jacob
• 0
1
vote
0
replies
945
views
Tutorial:
common mistakes in using spreadsheets
excel
spreadsheet
structured-data
updated 2.2 years ago by
Ram
45k • written 2.2 years ago by
Ming Tommy Tang
★ 4.7k
0
votes
0
replies
656
views
How to read count information from an old RGB based Agilent DNA array
CNV
Agilent
DNA
WGS
2.2 years ago by
K.patel5
▴ 150
4
votes
3
replies
2.0k
views
transcripts missing from tx2gene
R
transcriptome
DE
DESeq2
2.2 years ago by
dylannicoembros
• 0
2
votes
4
replies
1.6k
views
Is there a more elegant way to print the list of all regions from a bed file?
awk
2.2 years ago by
Axzd
▴ 80
4
votes
5
replies
1.6k
views
Keplen Meyer Curve Dropping to zero
R
SurvivalAnalysis
SurvFit
Surv
updated 2.2 years ago by
Shred
★ 1.6k • written 2.2 years ago by
Manuel Sokolov Ravasqueira
▴ 110
0
votes
2
replies
1.6k
views
DMR Analysis for RRBS: what annotation file to I use?
Methylation
RRBS
Annotation
updated 2.2 years ago by
Ming Tommy Tang
★ 4.7k • written 2.2 years ago by
embueno
• 0
0
votes
4
replies
1.0k
views
class codes x , lncRNA
class-codes
lncRNA
updated 2.2 years ago by
Ram
45k • written 2.2 years ago by
abductedbyaliens.vet
• 0
6
votes
8
replies
2.5k
views
How can I generate a list of 100 genomic intervals from bam files?
alignment
mapping
samtools
bam
genomics
updated 2.2 years ago by
GenoMax
154k • written 2.2 years ago by
kai_bio
▴ 60
0
votes
1
reply
1.3k
views
EMBOSS-FUZZNUC
fuzznuc
oligonucleotides
off-targets
microRNA
updated 2.2 years ago by
GenoMax
154k • written 2.2 years ago by
Ana
• 0
7
votes
5
replies
2.0k
views
Nextflow files not referenced correctly when using wildcard in a for loop
wildcard
Nextflow
2.2 years ago by
AshleeThomson
▴ 130
1
vote
2
replies
1.1k
views
DGEList error in EdgeR - Warning: Error in $: $ operator is invalid for atomic vectors
Limma
2.2 years ago by
shasabhi1
• 0
5
votes
8
replies
3.2k
views
6 follow
Convert files made for b37 into hg19 human reference?
GATK
Variant-Calling
Mutect2
updated 2.2 years ago by
Ming Tommy Tang
★ 4.7k • written 2.2 years ago by
Manuel Sokolov Ravasqueira
▴ 110
0
votes
2
replies
1.4k
views
PON and germline files for Mutect2 Tumor-only mode
GATK
Variant-Calling
Mutect2
updated 2.2 years ago by
Zhenyu Zhang
★ 1.3k • written 2.2 years ago by
Manuel
▴ 10
0
votes
6
replies
2.1k
views
Methylation Analysis - Missing Chromosome and Position Information for some CpG sites
methylation
updated 2.2 years ago by
Basti
★ 2.1k • written 2.2 years ago by
Irene
• 0
2
votes
8
replies
6.0k
views
Typical Volcano Plot for DGE
RNAseq
volcano
DGE
plots
updated 2.2 years ago by
ATpoint
89k • written 2.2 years ago by
fakeeha
• 0
0
votes
0
replies
632
views
News:
Course - Data Visualization in R with ggplot2
R
Data-Visualization
ggplot2
updated 2.2 years ago by
Ram
45k • written 2.2 years ago by
Physalia-courses
★ 2.6k
2
votes
3
replies
1.2k
views
converting .txt file to .ped and .map files
PLINK
updated 2.2 years ago by
Ram
45k • written 2.2 years ago by
jyothisrilok
• 0
0
votes
2
replies
1.0k
views
How to resample contacts data to lower bins
statistics
assembly
r
sequencing
binning
2.2 years ago by
kai_bio
▴ 60
1
vote
13
replies
2.6k
views
Unusual pattern in heatmap from ChIP-seq
chip-seq
heatmap
deeptools
2.2 years ago by
Marco Pannone
▴ 810
2
votes
7
replies
1.7k
views
Should we assume UMI-based scRNAseq data is not compositional?
compositional
scRNAseq
2.2 years ago by
cwwong13
▴ 40
6
votes
1
reply
843
views
16S vs shotgun tools
metagenomics
2.2 years ago by
anasjamshed
▴ 140
2
votes
9
replies
2.2k
views
Read length for single -ended RNA seq data analysis
read-length
fastq
updated 2.2 years ago by
Ram
45k • written 2.2 years ago by
vinaya
• 0
7
votes
5
replies
2.0k
views
GATK GetPileupSummaries Java heap space
GATK
Variant-Calling
GetPileupSummaries
updated 22 months ago by
Ram
45k • written 2.2 years ago by
Manuel Sokolov Ravasqueira
▴ 110
121,967 results • Page
225 of 2440
Recent Votes
GATK BaseRecalibrator error: input files reference and features have incompatible contigs
Answer: How to create a consensus of a contig with samtools or bbmap?
Comment: Getting just fastqc.zip file?
alternate allele frequency and minor allele frequency
Calculating minor allele frequency for GnomAD VCF file
Hiring FT Remote Nextflow engineer to build ML workflows for cancer genomics
Answer: Gene expression equivalent of polygenic risk score ?
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Comment: How to convert gff to Sequin format with gff3-to-tbl?
by
GenoMax
154k
So should your command not be (assuming these are the right files) ? $ gff3-to-tbl .../pharokka.gff .../Annotation/pharokka_cds_final…
Comment: How to convert gff to Sequin format with gff3-to-tbl?
by
marongiu.luigi
▴ 760
ADDENDUM: I have seen that pharokka already provides a tbl file; anyway, the question remains: if I needed to convert a gff to sequin with …
Comment: How to convert gff to Sequin format with gff3-to-tbl?
by
marongiu.luigi
▴ 760
Thank you, I have updated the title as suggested. But in the command, there a gff, a tsv, and a protein fasta. The list of files is: ``` $ …
Answer: How to convert gff to Sequin format?
by
GenoMax
154k
> $ gff3-to-tbl .../pharokka.gff .../Annotation/pharokka_cds_final_merged_output.tsv .../Consensus/reference.fasta .../Annotation/phanotate…
Comment: Errors with RSEM/bowtie2
by
GenoMax
154k
> Could this be an issue caused by the sequencing facility or just that they are in fact out of sync? We have no way to know. Did the sequ…
Comment: Differences between published differential gene expression results and own analy
by
vernonlim98
• 0
Have included the links to the papers I mentioned in another comment for reference!
Comment: Differences between published differential gene expression results and own analy
by
vernonlim98
• 0
These are the 2 papers I mentioned previously that used data other than raw counts for their analysis: https://onlinelibrary.wiley.com/doi/…
Comment: Collect COV file by BedCoverage
by
eshrakaali_p
• 0
Hello German , I am using clinCNV for WES and i faced the same error and this part of the error [1] "ERROR: your file with normal cove…
Comment: How to create a consensus of a contig with samtools or bbmap?
by
marongiu.luigi
▴ 760
sorry, I have mistaken samtools with spades... running `samtools view -h...` did the trick. Thank you.
Comment: Help with Ideathon
by
V K
• 0
Thank you for the response! Unfortunately this is completely independent and not part of a course. I was asking for some innovative ways to…
Answer: How to create a consensus of a contig with samtools or bbmap?
by
lieven.sterck
16k
You assembled a genome using samtools ???? that sounds very weird, if not impossible ... The header (SQ lines) is missing from your file b…
Answer: gnomad par region variants
by
benformatics
4.2k
The XX and XY counts are present on any given variants page.
Comment: Help with Ideathon
by
Mensur Dlakic
★ 30k
I don't see a single question here. Saying `I need your expert help in figuring out how I can make this analysis useful!` is too open-ended…
Comment: Differences between published differential gene expression results and own analy
by
ATpoint
89k
Please link the paper, lets see their methods. With human data it can well be that they included something like surrogate variables to damp…
Comment: Differences between published differential gene expression results and own analy
by
dsull
★ 7.7k
There are many ways to do normalization and one of the correct ways is simply to plug raw counts into deseq2 (the math that deseq2 uses to …
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