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121,974 results • Page
232 of 2440
Sort: Rank
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0
votes
0
replies
445
views
the Extreme Case in Global Alignment using Enumeration Method
principles
coursera
2.2 years ago by
Tully
• 0
3
votes
7
replies
2.7k
views
Normalization of Batch effect removal
ComBat
updated 2.2 years ago by
ATpoint
89k • written 2.2 years ago by
yoshifumimiya
▴ 50
3
votes
2
replies
1.2k
views
Blog:
Google launches Bard (and it fails the translation test :)
AI
updated 2.2 years ago by
Jesse
▴ 880 • written 2.2 years ago by
Michael
56k
0
votes
0
replies
616
views
Error while mapping data to reference using Symphony
Symphony
seurat
Mapping
R
2.2 years ago by
sidrah.maryam
▴ 70
3
votes
2
replies
988
views
many more ChIP-seq peaks called in 1 condition than the other
MACS2
ChIP-Seq
updated 2.2 years ago by
rfran010
★ 1.6k • written 2.2 years ago by
Pei
▴ 240
3
votes
7
replies
2.7k
views
VG Giraffe multi-mapped reads and definition for MAPQ score
vg
2.2 years ago by
Hendricks27
▴ 20
0
votes
0
replies
1.4k
views
Job:
Bioinformatics Postdoctoral Associates
Postdoc
updated 2.2 years ago by
Ram
45k • written 2.2 years ago by
lid
• 0
0
votes
17
replies
5.6k
views
Processing Fast5 files from ONT for direct RNA
Nanopore
Nanopolish
ELIGOS2
Fast5
Tombo
updated 2.2 years ago by
kenneditodd
▴ 50 • written 2.8 years ago by
Shagnik
• 0
0
votes
7
replies
1.7k
views
SNPeff problem
snpEff
updated 2.2 years ago by
Ram
45k • written 2.2 years ago by
Ed
• 0
3
votes
4
replies
1.8k
views
Trust in BQSR for AVITI
aviti
bqsr
2.2 years ago by
Ido Tamir
5.2k
2
votes
2
replies
1.1k
views
snakemake and snakefile question.
snakemake
updated 2.2 years ago by
Ram
45k • written 2.2 years ago by
Andy
▴ 120
3
votes
3
replies
1.4k
views
Where can I find the --chromosomes file for kallisto?
kallisto
updated 2.2 years ago by
GenoMax
154k • written 2.2 years ago by
bioinfo
▴ 160
3
votes
2
replies
1.2k
views
Mapping to mtDNA and then align the unmapped
mtDNA
Alignment
Samtools
Bowtie2
2.2 years ago by
DanielEB_fisk
▴ 20
0
votes
3
replies
1.1k
views
Retrieve rs IDs from chromossome location info on hg19 build
Variant-Annotation
rsIDs
updated 2.2 years ago by
GenoMax
154k • written 2.2 years ago by
elielsonveloso
• 0
0
votes
4
replies
1.4k
views
Downloading the fastq files did not well going; read in the fastq files are all the same
fastq
SRA
2.2 years ago by
Ken
• 0
0
votes
2
replies
1.3k
views
should remove unassigned genera in 16S rRNA sequencing analysis
16S
rRNA
metagenomics
sequencing
2.2 years ago by
zhangdengwei
▴ 210
0
votes
1
reply
1.9k
views
snpEff and SIFT calculation
snpEff
sift
updated 2.2 years ago by
estpallag
▴ 10 • written 5.5 years ago by
misterie
▴ 110
2
votes
1
reply
697
views
WGS database education
genetic-database
updated 2.2 years ago by
ATpoint
89k • written 2.2 years ago by
Amber Lisa
• 0
0
votes
0
replies
552
views
How to join and match two database lists, blastdb and list
linux
join
updated 2.2 years ago by
Ram
45k • written 2.2 years ago by
BATMAN
• 0
0
votes
0
replies
536
views
How to visualize incomplete viral genome ?
viral-genomes
denovo-assembly
updated 2.2 years ago by
Ram
45k • written 2.2 years ago by
mail2steff
▴ 70
0
votes
6
replies
2.6k
views
Adding an outgroup to a phylogeny: Steps and considerations
outgroup
alignment
2.2 years ago by
doggie
• 0
0
votes
3
replies
2.1k
views
R program - error installing ggplot2
R
updated 2.2 years ago by
seidel
11k • written 2.2 years ago by
Ehsan
• 0
1
vote
1
reply
1.9k
views
Seurat, FIndVariableFeatures(): vst not implemented yet
FindVariableFeatures
Seurat
vst
2.2 years ago by
Hatchet
▴ 10
3
votes
7
replies
2.0k
views
Double biological replication when using DESeq2
RNA-seq
DESeq2
Multi-region
updated 2.2 years ago by
ATpoint
89k • written 2.2 years ago by
350769816
▴ 10
2
votes
3
replies
2.4k
views
Can I liftover hs37d5 to hg38 using hg19ToHg38 chain file?
hs37d5
hg19
reference
hg38
PCAWG
updated 2.2 years ago by
Zhenyu Zhang
★ 1.3k • written 2.2 years ago by
ConvolutedGenome
▴ 60
11
votes
5
replies
1.8k
views
GOSemSim - difference between mgeneSim and mgoSim
gosemsim
similarity
updated 2.2 years ago by
DareDevil
★ 4.4k • written 2.2 years ago by
Giovanni
▴ 10
0
votes
0
replies
588
views
How to make Cicero Spider Plot
R
Cicero
IGV
2.2 years ago by
cthangav
▴ 110
0
votes
0
replies
649
views
Short read equivalent to long-read-tools.org
Sequencing
2.2 years ago by
ExtentHonest56
▴ 30
28
votes
13
replies
18k
views
11 follow
Tutorial:
Setting up Aspera Connect (ascp) on Linux and macOS
ascp
aspera
updated 23 months ago by
jude
• 0 • written 3.3 years ago by
ATpoint
89k
2
votes
1
reply
786
views
Help with an ATAC-seq cartoon
ATAC-seq
updated 2.2 years ago by
rfran010
★ 1.6k • written 2.2 years ago by
Chris
▴ 360
3
votes
5
replies
3.2k
views
Help understanding enhancer and promoter annotation
enhancers
GenomicRanges
annotatr
annotation
14 months ago by
alejandrarodrigu21
• 0
0
votes
0
replies
910
views
Seurat subset changes values in nFeature_RNA and nCount_RNA
Seurat
single-cell
updated 2.2 years ago by
Ram
45k • written 2.2 years ago by
Nikita
• 0
11
votes
6
replies
23k
views
6 follow
Remove cells from Seurat based on a list
scRNA-seq
Seurat
updated 2.2 years ago by
Ram
45k • written 5.4 years ago by
elb
▴ 260
0
votes
5
replies
1.6k
views
Multi omics data integration
multi-omics
integration
2.2 years ago by
samin415
• 0
0
votes
1
reply
898
views
Mset out of unmethylated and methylated signals (minfi)
minfi
methylation
updated 2.2 years ago by
Basti
★ 2.1k • written 2.2 years ago by
daria.kostiniuk
• 0
2
votes
3
replies
1.1k
views
How to Replicate JBrowse Plot
GenomeBrowser
JBrowse
Drosophila
FlyBase
updated 2.2 years ago by
cmdcolin
★ 4.3k • written 2.2 years ago by
serodyc
▴ 20
0
votes
0
replies
479
views
Unknown transgene sequence at Rosa26 locus
Rosa26
WGS
updated 2.2 years ago by
Ram
45k • written 2.2 years ago by
oneillcg
• 0
0
votes
1
reply
914
views
Differential expression of Long non coding RNA
SumarizedExperiment
updated 2.2 years ago by
GenoMax
154k • written 2.2 years ago by
amrendra.niper
• 0
2
votes
0
replies
3.8k
views
Tutorial:
How to read multiple matrices from GEO into R and make multiple Seurat objects and merge them into a single object.
unix
Seurat
single-cell
rstats
updated 2.2 years ago by
Ram
45k • written 2.2 years ago by
Ming Tommy Tang
★ 4.7k
0
votes
0
replies
756
views
using CNVKit with genome wide CNV backbone spike-in
cnvkit
cnv
cancer
ngs
2.2 years ago by
erikt
▴ 30
2
votes
4
replies
1.8k
views
gff3ToGenePred
gff3
annovar
2.2 years ago by
bestone
▴ 30
0
votes
0
replies
545
views
Input fo Metaxcan
predixcan
twas
2.2 years ago by
Genotepes
▴ 950
0
votes
0
replies
571
views
snps being shared by gene in different tissues
mechanism
shared
colocalization
snp
tissues
2.2 years ago by
rheab1230
▴ 150
5
votes
4
replies
1.3k
views
Is there a way to prove that two VCFs came from the same person?
vcf
identification
individual
updated 2.2 years ago by
Ming Tommy Tang
★ 4.7k • written 2.2 years ago by
Lee
▴ 10
0
votes
3
replies
2.5k
views
Query regarding cytoscape installation and uninstallation in ubuntu
Cytoscape
ubuntu
updated 2.2 years ago by
Manuela
• 0 • written 2.2 years ago by
microorganism_001
▴ 30
19
votes
7
replies
8.4k
views
Tutorial:
scRNA-seq CITE-seq-count bioinformatics
CITE-seq-count
scRNA-seq
RNA-Seq
updated 2.2 years ago by
ATpoint
89k • written 5.5 years ago by
colindaven
8.0k
0
votes
0
replies
505
views
Can I repeat markers in different cell types in the MCP-counter custom panel?
MCP-counter
2.2 years ago by
RM123
▴ 10
0
votes
0
replies
488
views
Error while trying to plot PCoA into stat_ellipse
qiime2R
stat_ellipse
ggplot2
2.2 years ago by
Lívia
• 0
3
votes
4
replies
2.5k
views
Qualimap multi-bamqc input file
Alignment
Qualimap
bam
bamqc
updated 2.2 years ago by
DBScan
▴ 530 • written 2.2 years ago by
DanielEB_fisk
▴ 20
22
votes
14
replies
28k
views
11 follow
searching reads with a certain sequence in fastq file
grep
fastq
updated 2.2 years ago by
elina2410
• 0 • written 10.5 years ago by
sumithrasank75
▴ 140
121,974 results • Page
232 of 2440
Recent Votes
Answer: infercnv error at STEP 18 - file descriptor is too large for select()
A: bwa for multiple fastq files
A: bwa for multiple fastq files
Comment: Issue about generating EMBL Flat file for ENA submission
Answer: Gene expression equivalent of polygenic risk score ?
Which aligner is more suitable for ONT R10.4.1 Dorado-corrected reads: minimap2 or winnowmap?
A: What to use for a measure of distance between two sequences?
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Recent Replies
Comment: Quantification using salmon in alignment-based mode after minimap2 run
by
Rob
7.1k
As @atpoint suggests, you must align against the transcriptome. Also, the other relevant flags should be set (i.e. `--secondary=no` will di…
Answer: Quantification using salmon in alignment-based mode after minimap2 run
by
ATpoint
89k
Yes, must strictly be transcriptome. Reference from developer: https://www.biostars.org/p/9556364/
Comment: Errors with RSEM/bowtie2
by
Olivia
• 0
Yes, they removed the adapters, so I did not have to do extra steps for this (other than Trimmomatic within Trinity to get rid of short con…
Answer: infercnv error at STEP 18 - file descriptor is too large for select()
by
yura.grabovska
▴ 830
Noticed that running `infercnv::CreateInfercnvObject()` generates a warning: ``` WARN [2025-10-06 14:43:38] Please use "options(scipen = …
Comment: Which aligner is more suitable for ONT R10.4.1 Dorado-corrected reads: minimap2
by
tungsega
▴ 10
Thank you for your reply. I’m currently trying to perform alignments using both aligners, but I wanted to ask if anyone has conducted a si…
Comment: Which aligner is more suitable for ONT R10.4.1 Dorado-corrected reads: minimap2
by
colindaven
8.0k
Good summary. I never tried winnowmap despite it's apparent advantages. If you have really repeat rich regions like centromeres that it may…
Comment: Need Help : JGI IMG Bulk Download
by
GenoMax
154k
Please post direct links to software you mention. Not sure why you are using LinkedIn short URL's. Historically downloads from JGI have be…
Comment: Hifiasm is getting killed while trying to assemble a genome
by
pranavdatar01
• 0
This is the paper: https://doi.org/10.3389/fevo.2022.850817 (Genome of Varanus salvator macromaculatus (Asian Water Monitor) Reveals Adapta…
Comment: How to create a consensus of a contig with samtools or bbmap?
by
lieven.sterck
16k
great to hear! and yes, spades in stead of samtools makes much more sense :-)
Answer: Nextflow: How to format input tuple for STAR_ALIGN process with STAR index direc
by
Pierre Lindenbaum
166k
> align_ch returns tuples like [sample_name, [read1, read2]]. I want aligned_input tuples to look like [index_dir, sample1, read1, read2]. …
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…
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