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121,967 results • Page
222 of 2440
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Votes
Replies
0
votes
2
replies
8.8k
views
Tool:
The script to install the required packages for gene expression analysis using DESeq2 for downstream analysis and visualization
R
RNAseq
installation
DESeq2
2.2 years ago by
Aditya naman
• 0
2
votes
5
replies
1.7k
views
how to compare mapping of WES samples to human pangenome?
WES
pangenome
vg
2.1 years ago by
bitpir
▴ 250
1
vote
1
reply
705
views
How to read PAR variants in chr23 from .bgen file?
PAR
bgen
updated 2.1 years ago by
Ram
45k • written 2.2 years ago by
David
• 0
0
votes
2
replies
971
views
Encode eCLIP-seq bed.gz header name
eclip-seq
encode
bed.gz
updated 2.2 years ago by
GenoMax
154k • written 2.2 years ago by
u0693520
• 0
0
votes
0
replies
848
views
Error in h(simpleError(msg, call)) in monocle2
pseudotime
scRNAseq
monocle2
2.2 years ago by
abmmki
• 0
1
vote
1
reply
1.0k
views
Annotate VCF with RepeatMasker
RepeatMasker
VCF
annotation
updated 2.2 years ago by
barslmn
★ 2.4k • written 2.2 years ago by
Aiswarya
▴ 20
7
votes
0
replies
957
views
Tutorial:
Polygenic Risk Score Calculation
genetic-burden
r
prs
ggplot
glm
2.1 years ago by
barslmn
★ 2.4k
1
vote
0
replies
1.3k
views
Tool:
Create realistic VCF genomic data in just a few lines of Python code
genomic
linkage
python
vcf
tool
disequilibrium
2.2 years ago by
Rémy
▴ 10
1
vote
1
reply
1.2k
views
CHOPCHOP command line
sgRNA
chopchop
updated 2.2 years ago by
GenoMax
154k • written 2.6 years ago by
gernophil
▴ 130
8
votes
5
replies
3.2k
views
Alternative splicing events
Leafcutter
leafviz
Splicing
events
updated 15 months ago by
Sara
▴ 40 • written 2.9 years ago by
Ezhil La
▴ 40
0
votes
4
replies
1.6k
views
snRNA seq analysis - huge computational demand due to large number of entries
seq
snRNA
updated 2.2 years ago by
predeus
★ 2.1k • written 2.2 years ago by
applepie
▴ 10
2
votes
2
replies
2.2k
views
Co-expression of markers in single cells using scanpy
scanpy
co-expression
single-cell
2.1 years ago by
A.rex2
• 0
0
votes
3
replies
1.1k
views
Can retrogenes keep their introns?
retrotransposition
duplication
retrogenes
updated 2.2 years ago by
LChart
5.1k • written 2.2 years ago by
codoncity
• 0
2
votes
8
replies
3.5k
views
METAL-Random
Random-effect
METAL
updated 13 months ago by
Ram
45k • written 3.5 years ago by
kris
▴ 10
0
votes
0
replies
601
views
segemehl: How does the arrangement of references influence mapping results?
segemehl
mapping
sequencing
2.2 years ago by
Cristian
• 0
0
votes
2
replies
1.1k
views
Skewed qq plot from logistic regression
R
glm
qqplot
2.2 years ago by
graeme.thorn
▴ 110
5
votes
7
replies
2.5k
views
How to identify which genome the variations in the pan-genome graph originate from
vg
2.2 years ago by
Wenke
• 0
4
votes
5
replies
2.5k
views
why does vg convert doesn't work?
vg
updated 2.2 years ago by
GenoMax
154k • written 2.2 years ago by
Michal
• 0
0
votes
3
replies
1.3k
views
molecular docking for a ligand to multi protein
molecular-docking
autodock-vina
updated 2.2 years ago by
Aditya naman
• 0 • written 2.2 years ago by
iamsmor
• 0
8
votes
15
replies
2.7k
views
Filtering parasite reads from host reads
tools
RNA-seq
updated 2.2 years ago by
GenoMax
154k • written 2.2 years ago by
m.habib
• 0
4
votes
5
replies
1.4k
views
Next generation sequencing
R
NGS
written 2.2 years ago by
Farha
▴ 10
2
votes
0
replies
559
views
How to perform functional enrichment of Metabolites?
PerformPSEA
metaboanalyst
GSEA
metabolites
2.2 years ago by
DareDevil
★ 4.4k
0
votes
2
replies
1.2k
views
CUDA error when I run megalodon (2.4.1) and guppy (6.0.1+652ffd1) with GPU support.
Megalodon
ONT
GPU
nanopore
Guppy
updated 2.2 years ago by
GenoMax
154k • written 2.2 years ago by
1595952559
• 0
0
votes
5
replies
1.2k
views
How to deal with two dataset of RNA expression
Affymetrix
microarray
RNA-seq
2.2 years ago by
Yibin
• 0
2
votes
3
replies
2.0k
views
How to find the coverage of the assembled contigs of the PacBio long reads?
PacBio
assembly
coverage
updated 2.2 years ago by
liorglic
★ 1.5k • written 2.2 years ago by
rj.rezwan
▴ 20
0
votes
0
replies
1.9k
views
Tutorial:
How to preprocess and visualize beautifully scRNA-seq with omicverse?
scRNA-seq
seurat
scanpy
Python
2.2 years ago by
Starlitnightly
• 0
0
votes
5
replies
1.6k
views
bamCoverage fails in bam files with large number of small contigs in headers
bamCoverage
updated 2.2 years ago by
colindaven
8.0k • written 2.2 years ago by
sarahmanderni
▴ 130
1
vote
1
reply
995
views
log2Fold Change as input for k-means analysis
gene-analysis
RNA-seq
k-means
updated 2.2 years ago by
rfran010
★ 1.6k • written 2.2 years ago by
concetta
▴ 10
0
votes
0
replies
702
views
Highly degenerate primers and BLAST
blast
2.2 years ago by
Philipp Bayer
8.9k
0
votes
2
replies
945
views
Question with manipulating OD gene list when running PCA
Pagoda2
PCA
RNA-seq
Seurat
2.2 years ago by
K
• 0
4
votes
4
replies
1.2k
views
I cannot install anaconda on ubuntu 22.04
ubuntu
anaconda
Conda
updated 2.2 years ago by
Ram
45k • written 2.2 years ago by
Omar
▴ 10
0
votes
5
replies
1.6k
views
DESEQ2 analysis - PCA plot
RNA-seq
differential-expression
deseq2
updated 2.2 years ago by
bkleiboeker
▴ 370 • written 2.2 years ago by
shome
▴ 10
2
votes
3
replies
997
views
Downloading Microsyntenic Fasta Sequences with Varying Chromosome Formats
microsyntenic-region
fasta
oma
chromosomes
2.2 years ago by
Nicolas
• 0
0
votes
2
replies
1.1k
views
How to assess quality of publicly available microarray data
control
probes
affymetrix
2.2 years ago by
Will
• 0
1
vote
4
replies
1.3k
views
Matched samples in Deseq2
RNA-seq
deseq2
2.2 years ago by
noodlejackson
▴ 40
1
vote
0
replies
711
views
News:
NIAID Data Ecosystem Discovery Portal
databases
data
opendata
api
2.2 years ago by
ehaag
▴ 100
2
votes
8
replies
1.6k
views
converting Gene ID to GeneSymbols
NCBI
Gene-Symbol
updated 2.2 years ago by
Ram
45k • written 2.2 years ago by
Mehvi khan
• 0
0
votes
2
replies
1.1k
views
How does bcftools decide what sample name to assign when calling variants?
bcftools
variant-calling
2.2 years ago by
Paul
• 0
5
votes
11
replies
1.8k
views
Make heatmap for RNA-seq with non replicate
RNA-seq
updated 2.2 years ago by
Ram
45k • written 2.2 years ago by
Chris
▴ 360
0
votes
5
replies
2.8k
views
Scanning a genomic region for TFBS
Transcription
Factor
TF
TFBS
updated 2.2 years ago by
Alex Reynolds
36k • written 2.2 years ago by
Mohammed
▴ 10
0
votes
0
replies
754
views
How to decide number of features
object
number
features
Seurat
of
2.2 years ago by
Andy
▴ 120
0
votes
5
replies
2.4k
views
Revisit where to find CCLE RNAseq in FPKM or RPKM using RSEM values to perform normalization- as was never answered usefully
RNA
CCLE
updated 2.2 years ago by
GenoMax
154k • written 2.2 years ago by
Mitchell.frederick
▴ 10
0
votes
0
replies
780
views
News:
Course - Structural Variant detection and comparison
SVs
Structural-Variants
updated 2.2 years ago by
Ram
45k • written 2.2 years ago by
Physalia-courses
★ 2.6k
2
votes
4
replies
1.6k
views
fasttree running problem
fasttree
2.2 years ago by
chopinone
• 0
0
votes
2
replies
1.0k
views
AWS for Kraken2 custom database
metagenomics
ncbi
kraken2
cloud
aws
2.2 years ago by
Natalia
• 0
1
vote
3
replies
1.4k
views
From VCF to AVINPUT
convert2annovar.pl
annovar
updated 2.2 years ago by
Pierre Lindenbaum
166k • written 2.2 years ago by
Can Abdullah
• 0
0
votes
2
replies
1.0k
views
Map to get cpg probe id provided chr, start and end position
methylation
genomic
annotation
TCGA
2.2 years ago by
dilrajkaur766
• 0
2
votes
4
replies
1.1k
views
I have a FASTA file. I want to extract from some sequence using seqtk. What should be the command for it?
WGS
2.2 years ago by
Mustafa
• 0
0
votes
5
replies
3.3k
views
How to solve STAR tools error : quality string length is not equal to sequence length ?
STAR
illumina
sequencing
RNAseq
Alignment
updated 2.2 years ago by
GenoMax
154k • written 2.2 years ago by
Aditya naman
• 0
0
votes
0
replies
454
views
Looking for an Alternative of SELECTON/2.4 for my aligned data to calculate position wise KaKs values?
KaKs
selecton
updated 2.2 years ago by
Ram
45k • written 2.2 years ago by
Muhammad
• 0
121,967 results • Page
222 of 2440
Recent Votes
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 ?
A: TRF output to .gff file
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Recent Replies
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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