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120,868 results • Page
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4
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10
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57
views
Batch correction RNA-seq analysis
rna-seq
ComBat-seq
batch
correction
updated just now by
GenoMax
150k • written 1 hour ago by
ka132
• 0
0
votes
5
replies
253
views
Depth in Cram file does not match depth in VCF file
IGV
of
Depth
SNV
coverage
updated 2 hours ago by
Istvan Albert
102k • written 1 day ago by
shu8
• 0
1
vote
1
reply
38
views
Tools for clustering genes rather than samples for bulk RNA-seq
time
Bulk
RNA-seq
course
clustering
updated 2 hours ago by
i.sudbery
21k • written 2 hours ago by
ATS
• 0
0
votes
2
replies
64
views
News:
Wolfram tech for bio data analysis
plots
statistics
databases
ai
updated 53 minutes ago by
GenoMax
150k • written 4 hours ago by
dk7258859
• 0
0
votes
1
reply
164
views
what database should I use for de novo genome in AUGUSTUS
genome
AUGUSTUS
galaxy
annotation
updated 3 hours ago by
lieven.sterck
15k • written 2 days ago by
Jl
• 0
1
vote
3
replies
92
views
Is there a tool to obtain GO terms for thousands of genes at once?
permutations
Genes
updated 4 hours ago by
GenoMax
150k • written 5 hours ago by
Ana
• 0
0
votes
1
reply
65
views
cant make the correct matrix
logfc
csv
updated 5 hours ago by
lieven.sterck
15k • written 6 hours ago by
Naila
• 0
835
votes
169
replies
172k
views
110 follow
News:
The Biostar Handbook. A bioinformatics e-book for beginners.
training
handbook
updated 6 months ago by
Biostar
3.4k • written 8.3 years ago by
Istvan Albert
102k
1
vote
4
replies
100
views
FIxing Gene Models in Funannotate
genomics
funannotate
fungus
annotation
4 hours ago by
SomeOne
▴ 170
1
vote
7
replies
167
views
How to Make Cell Order identical Between Two Seurat Objects in R?
R
seurat
scRNA-seq
updated 6 hours ago by
yura.grabovska
▴ 750 • written 8 hours ago by
zhang616123
• 0
0
votes
2
replies
85
views
Assign different color in same section of Chord diagram in R
Chart
R
Diagram
Plot
Chord
4 hours ago by
Jonathan Yoou
▴ 70
0
votes
0
replies
46
views
Issues with vg surject into paths
vg
7 hours ago by
Rugare
• 0
0
votes
0
replies
48
views
News:
Live Online course: Introduction to Python, April, 2025
python
programming
course
9 hours ago by
soledad.esteban
• 0
0
votes
4
replies
128
views
Niormalization process in creating heatmap
Z
heatmap
score
Normalization
updated 11 hours ago by
ATpoint
87k • written 11 hours ago by
ZuelTech
• 0
1
vote
14
replies
383
views
Lacking exons in gtf file of a virus' genome
gtf
exon
Mapping
Hazara
VirusGenome
updated 11 hours ago by
colindaven
7.3k • written 1 day ago by
ZuelTech
• 0
1
vote
4
replies
812
views
Should I process two complete sets of 10x single-cell multiomics sequencing files from one donor together or separately?
10x_multiome
ENCODE
cellranger_arc
updated 17 hours ago by
swbarnes2
14k • written 2 days ago by
Wu-Sheng Zhang
• 0
1
vote
4
replies
187
views
Count matrices plotting
count
matrix
scanpy
8 hours ago by
NIkita
• 0
1
vote
6
replies
133
views
Filter snRNA-seq .fastq files based on barcodes
snRNA-seq
scRNA-seq
FASTQ
bbmap
updated 1 hour ago by
GenoMax
150k • written 19 hours ago by
connorjfausto
▴ 30
0
votes
1
reply
114
views
Defining Sex Chromosomes in PLINK for a Camel Genome
plink
vcf
updated 20 hours ago by
chrchang523
11k • written 1 day ago by
Smilesky
• 0
0
votes
0
replies
59
views
Why is the IC50 of the low-risk group always lower than that of the high-risk group?
OncoPredict
21 hours ago by
nuorain
▴ 40
0
votes
0
replies
73
views
News:
Introduction to Epigenomics course
Epigenomics
RNA-seq
ATAC-seq
Chip-seq
HI-C
1 day ago by
Physalia-courses
★ 2.6k
0
votes
2
replies
130
views
Remove batch effect RnaSeq (RUVg)
ruvg
batch
rnaseq
remove
7 hours ago by
aLex97
• 0
0
votes
0
replies
78
views
Annotation of CpG, DMRs and DMPs with MethylKit and Genomation in R
dmp
methylkit
dmr
CpG
1 day ago by
egascon
▴ 60
1
vote
0
replies
166
views
Tool:
A rust binding for pairwise/multiple sequence aligner: bsalign-rs
bsalign
alignment
16 hours ago by
dwpeng
▴ 120
0
votes
2
replies
252
views
Perform DEGs with pyDESeq2 in CCLE Melanoma Data But Contains Negative Values
DEG
CCLE
Melanoma
pyDESeq2
3 days ago by
mete.han.celebi
• 0
0
votes
0
replies
167
views
energy minimisation
Energy
updated 3 days ago by
Pierre Lindenbaum
165k • written 3 days ago by
swarnadurga66666m
• 0
0
votes
1
reply
195
views
How to concatenate different domains in the target database identified by hmmsearch
multiple
domains
hmmsearch
updated 3 days ago by
GenoMax
150k • written 3 days ago by
Yongjie Zhang
▴ 110
0
votes
1
reply
202
views
How to filter Hmmsearch alignment
Hmmsearch
updated 3 days ago by
Mensur Dlakic
★ 29k • written 3 days ago by
Yongjie Zhang
▴ 110
2
votes
3
replies
2.3k
views
Defining residues as buried or exposed based in ASAs/RSAs
structural-bioinformatics
protein-biology
updated 3 days ago by
Dan A
• 0 • written 3.7 years ago by
Agenor Neto
▴ 10
1
vote
1
reply
227
views
Understanding Re-use of Query Sequences in Long Read Alignments
Alignment
PacBio
pbmm2
Minimap2
updated 3 days ago by
LauferVA
4.6k • written 3 days ago by
Charles-Alexandre Roy
▴ 50
0
votes
0
replies
159
views
Question about `vg construct`
vg
3 days ago by
zhengluo
• 0
0
votes
2
replies
293
views
Discrepancy between BAM and vcf
discrepancy
vcf
DRAGEN
updated 4 days ago by
Istvan Albert
102k • written 4 days ago by
louis-gil
• 0
2
votes
1
reply
418
views
Question about `vg giraffe`
vg
updated 4 days ago by
GenoMax
150k • written 5 days ago by
zhengluo
• 0
0
votes
1
reply
491
views
Difference in mapping rate when aligned with mapper.pl of miReep2 and bowtie1
small-RNASeq
miRNASeq
bowtie
miRDeep2
updated 4 days ago by
Ram
45k • written 9 months ago by
MIKA
• 0
3
votes
3
replies
379
views
How to align library of highly similar sequences
MPRA
variant
alignment
BWA
SNV
22 hours ago by
rustyshackleford
• 0
0
votes
3
replies
1.6k
views
How to introduce normalized and scaled seurat data into monocle 3?
Monocle
scRNA-seq
Seurat
updated 4 days ago by
Bastien Hervé
6.2k • written 22 months ago by
Sun
• 0
0
votes
1
reply
241
views
Reannotation of complete bacterial genome sequence
re-annotation
genome
whole
Automated
updated 1 day ago by
Juke34
9.2k • written 5 days ago by
csag6433
• 0
0
votes
2
replies
809
views
What are the best tools for quantifying allele-specific expression from bulk RNA-seq data these days?
ase
phASER
allele
gene
gatk
updated 4 days ago by
GenoMax
150k • written 5 days ago by
Paulo
• 0
3
votes
4
replies
3.3k
views
Lift over of GWAS summary stat file from Hg38 to Hg19
Hg38
linux
Liftover
GWAS
Hg19
updated 3 days ago by
Mllepnos
• 0 • written 3.8 years ago by
AVA
▴ 40
8
votes
3
replies
376
views
How do I install Terminal on Windows?
Terminal
updated 5 days ago by
5heikki
11k • written 5 days ago by
phyms
• 0
1
vote
1
reply
243
views
Mapping reversion mutations
NGS
reversion
mutation
updated 5 days ago by
Ram
45k • written 5 days ago by
reddyraghuveer664
• 0
0
votes
0
replies
201
views
Issue with Fetching Population Allele Frequency in gnomAD GraphQL API
allelle
frequency
api
GraphQL
gnomad
5 days ago by
DareDevil
★ 4.4k
0
votes
1
reply
245
views
Attempts to demultiplex long reads from .pod5 result in unclassified reads
dorado
sequencing
Long-read
demultiplex
updated 5 days ago by
GenoMax
150k • written 5 days ago by
Placeholder@12654926
• 0
0
votes
1
reply
274
views
Issue with BSgenomeForge::forgeBSgenomeDataPkgFromNCBI
R
BSgenomeForge
BSgenome
NCBI
updated 5 days ago by
ATpoint
87k • written 5 days ago by
noodle
▴ 650
1
vote
1
reply
286
views
Batch effect or biological difference
Batch-effect
updated 5 days ago by
Ram
45k • written 5 days ago by
cynthier
• 0
3
votes
2
replies
330
views
Inconsistency between VCF and HGVS
VEP
5 days ago by
Senanu
▴ 30
0
votes
1
reply
219
views
VCFtools + easySFS snp # discordance
RADtags
vcftools
updated 1 hour ago by
Istvan Albert
102k • written 5 days ago by
laurasachica7
• 0
0
votes
4
replies
3.2k
views
Generating Multiple Alignment Format file (Maf)
maf
multiple-alignment
mafft
updated 5 days ago by
Ram
45k • written 8.3 years ago by
roz_safavi
• 0
3
votes
6
replies
489
views
STAR: Paired alignment gets ~18% unmapped (too short), but single reads get >90% mapping
paired-end
star
rnaseq
5 days ago by
Davor
• 0
1
vote
0
replies
321
views
Job:
bioinformatician position, Ohio State University, Columbus, USA
bioinformatician
updated 6 days ago by
GenoMax
150k • written 6 days ago by
ilaria.palmisano
▴ 10
120,868 results • Page
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Comment: Batch correction RNA-seq analysis
Comment: Batch correction RNA-seq analysis
Answer: Batch correction RNA-seq analysis
Comment: Batch correction RNA-seq analysis
Answer: Tools for clustering genes rather than samples for bulk RNA-seq
Answer: Is there a tool to obtain GO terms for thousands of genes at once?
Answer: FIxing Gene Models in Funannotate
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Comment: Batch correction RNA-seq analysis
by
ka132
• 0
Unfortunately, I just found out the libraries were prepped separately as well. Thanks for the advice!
Comment: Batch correction RNA-seq analysis
by
ka132
• 0
Well, dangit - I just heard back and the same sequencer was used but library prep was done separately. Bummer. Thanks for the assistance.
Comment: Batch correction RNA-seq analysis
by
jared.andrews07
★ 18k
Batch correction as you mention shouldn't even run, I expect ComBat-seq will yell at you about confounded covariates if you try. But as me…
Comment: Batch correction RNA-seq analysis
by
ka132
• 0
The actual experiment and collection of samples were done at same time. Library prep was definitely done by same person using same protocol…
Comment: Batch correction RNA-seq analysis
by
GenoMax
150k
There should be no appreciable batch effect because of sequencing, as long as following is true. The same sequencer (or at least type i.e. …
Comment: Batch correction RNA-seq analysis
by
ka132
• 0
yeah.... this is what I was afraid of. I wish this was a lesson that I needed to learn, but again I had no input on the processing up to th…
Comment: Batch correction RNA-seq analysis
by
ka132
• 0
Just sequencing, no common control unfortunately.
Comment: Batch correction RNA-seq analysis
by
GenoMax
150k
> samples were **run** It would help if you clarify "run" part further. What exact part of the experiment was done in two batches. Full …
Comment: Wolfram tech for bio data analysis
by
GenoMax
150k
> Part of the motivation for this is that many universities have a full site-wide license for our software Is there a publicly available l…
Answer: Batch correction RNA-seq analysis
by
jared.andrews07
★ 18k
If you have no overlap between batches, there are unfortunately no real options. The experiment is confounded. Consider this an expensive a…
Comment: Filter snRNA-seq .fastq files based on barcodes
by
GenoMax
150k
`filterbyname.sh` only works based on information that is found in the **fastq header**. As you can see the barcodes you have are not in th…
Comment: Filter snRNA-seq .fastq files based on barcodes
by
GenoMax
150k
> How would I use the filtered bam files to get the fastq? If you have the BAM files you can simply use `samtools fastq your.bam` with app…
Comment: VCFtools + easySFS snp # discordance
by
Istvan Albert
102k
this would not be easy to answer without seeing your VCF file - maybe you could share that VCF and people can take a look at it.
Comment: Filter snRNA-seq .fastq files based on barcodes
by
connorjfausto
▴ 30
Yes these barcodes came from a Seurat Object aligned from `cellranger count`, I'll change the `.csv` file with your corrections and try. I …
Comment: Filter snRNA-seq .fastq files based on barcodes
by
connorjfausto
▴ 30
Thanks for the response! Here's an example of an out when i input `zcat fq_r1.fastq.gz | head -n 10` ``` @A00738:690:HCNMKDSX7:3:1101:2102…
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