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120,848 results • Page
1 of 2417
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Votes
Replies
0
votes
3
replies
76
views
Depth in Cram file does not match depth in VCF file
IGV
of
Depth
SNV
coverage
updated 1 hour ago by
karl.stamm
4.1k • written 5 hours ago by
shu8
• 0
1
vote
0
replies
91
views
Tool:
A rust binding for pairwise/multiple sequence aligner: bsalign-rs
bsalign
alignment
13 hours ago by
dwpeng
▴ 120
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
0
votes
0
replies
71
views
what database should I use for de novo genome in AUGUSTUS
genome
AUGUSTUS
galaxy
annotation
1 day ago by
Jl
• 0
0
votes
3
replies
432
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 8 hours ago by
GenoMax
150k • written 1 day ago by
Wu-Sheng Zhang
• 0
0
votes
2
replies
162
views
Perform DEGs with pyDESeq2 in CCLE Melanoma Data But Contains Negative Values
DEG
CCLE
Melanoma
pyDESeq2
1 day ago by
mete.han.celebi
• 0
0
votes
0
replies
98
views
energy minimisation
Energy
updated 1 day ago by
Pierre Lindenbaum
165k • written 1 day ago by
swarnadurga66666m
• 0
0
votes
1
reply
123
views
How to concatenate different domains in the target database identified by hmmsearch
multiple
domains
hmmsearch
updated 1 day ago by
GenoMax
150k • written 1 day ago by
Yongjie Zhang
▴ 110
0
votes
1
reply
127
views
How to filter Hmmsearch alignment
Hmmsearch
updated 1 day ago by
Mensur Dlakic
★ 29k • written 1 day ago by
Yongjie Zhang
▴ 110
2
votes
3
replies
2.2k
views
Defining residues as buried or exposed based in ASAs/RSAs
structural-bioinformatics
protein-biology
updated 1 day ago by
Dan A
• 0 • written 3.7 years ago by
Agenor Neto
▴ 10
1
vote
1
reply
156
views
Understanding Re-use of Query Sequences in Long Read Alignments
Alignment
PacBio
pbmm2
Minimap2
updated 1 day ago by
LauferVA
4.6k • written 2 days ago by
Charles-Alexandre Roy
▴ 50
0
votes
0
replies
96
views
Question about `vg construct`
vg
1 day ago by
zhengluo
• 0
0
votes
2
replies
215
views
Discrepancy between BAM and vcf
discrepancy
vcf
DRAGEN
updated 2 days ago by
Istvan Albert
102k • written 2 days ago by
louis-gil
• 0
2
votes
1
reply
345
views
Question about `vg giraffe`
vg
updated 2 days ago by
GenoMax
150k • written 3 days ago by
zhengluo
• 0
0
votes
1
reply
436
views
Difference in mapping rate when aligned with mapper.pl of miReep2 and bowtie1
small-RNASeq
miRNASeq
bowtie
miRDeep2
updated 2 days ago by
Ram
45k • written 9 months ago by
MIKA
• 0
1
vote
2
replies
269
views
How to align library of highly similar sequences
MPRA
variant
alignment
BWA
SNV
updated 2 days ago by
ATpoint
87k • written 3 days ago by
rustyshackleford
• 0
0
votes
3
replies
1.5k
views
How to introduce normalized and scaled seurat data into monocle 3?
Monocle
scRNA-seq
Seurat
updated 2 days ago by
Bastien Hervé
6.2k • written 22 months ago by
Sun
• 0
0
votes
0
replies
152
views
Reannotation of complete bacterial genome sequence
re-annotation
genome
whole
Automated
3 days ago by
csag6433
• 0
0
votes
2
replies
725
views
What are the best tools for quantifying allele-specific expression from bulk RNA-seq data these days?
ase
phASER
allele
gene
gatk
updated 3 days ago by
GenoMax
150k • written 3 days ago by
Paulo
• 0
3
votes
4
replies
3.2k
views
Lift over of GWAS summary stat file from Hg38 to Hg19
Hg38
linux
Liftover
GWAS
Hg19
updated 2 days ago by
Mllepnos
• 0 • written 3.8 years ago by
AVA
▴ 40
8
votes
3
replies
302
views
How do I install Terminal on Windows?
Terminal
updated 3 days ago by
5heikki
11k • written 3 days ago by
phyms
• 0
1
vote
1
reply
188
views
Mapping reversion mutations
NGS
reversion
mutation
updated 3 days ago by
Ram
45k • written 3 days ago by
reddyraghuveer664
• 0
0
votes
0
replies
148
views
Issue with Fetching Population Allele Frequency in gnomAD GraphQL API
allelle
frequency
api
GraphQL
gnomad
3 days ago by
DareDevil
★ 4.4k
0
votes
1
reply
189
views
Attempts to demultiplex long reads from .pod5 result in unclassified reads
dorado
sequencing
Long-read
demultiplex
updated 3 days ago by
GenoMax
150k • written 3 days ago by
Placeholder@12654926
• 0
0
votes
1
reply
216
views
Issue with BSgenomeForge::forgeBSgenomeDataPkgFromNCBI
R
BSgenomeForge
BSgenome
NCBI
updated 3 days ago by
ATpoint
87k • written 3 days ago by
noodle
▴ 640
1
vote
1
reply
225
views
Batch effect or biological difference
Batch-effect
updated 3 days ago by
Ram
45k • written 3 days ago by
cynthier
• 0
3
votes
2
replies
269
views
Inconsistency between VCF and HGVS
VEP
3 days ago by
Senanu
▴ 30
0
votes
0
replies
163
views
VCFtools + easySFS snp # discordance
RADtags
vcftools
updated 4 days ago by
GenoMax
150k • written 4 days ago by
laurasachica7
• 0
0
votes
4
replies
3.2k
views
Generating Multiple Alignment Format file (Maf)
maf
multiple-alignment
mafft
updated 4 days ago by
Ram
45k • written 8.3 years ago by
roz_safavi
• 0
3
votes
6
replies
414
views
STAR: Paired alignment gets ~18% unmapped (too short), but single reads get >90% mapping
paired-end
star
rnaseq
3 days ago by
Davor
• 0
1
vote
0
replies
247
views
Job:
bioinformatician position, Ohio State University, Columbus, USA
bioinformatician
updated 4 days ago by
GenoMax
150k • written 4 days ago by
ilaria.palmisano
▴ 10
3
votes
4
replies
328
views
Coverage drop at assembly ends
bowtie2
bw-mem
alignment
minimap2
updated 4 days ago by
GenoMax
150k • written 4 days ago by
alenew.am
▴ 10
1
vote
4
replies
405
views
How to identify additional SNPs on EPICv2
SNPs
methylation
EPIC
4 days ago by
Basti
★ 2.0k
0
votes
1
reply
226
views
jcvi:ValueError: A total of 0 anchor was found. Aborted.
jcvi
Collinearity
updated 4 days ago by
Ram
45k • written 4 days ago by
JieQY
• 0
0
votes
5
replies
445
views
SNPcheck alternative
SNPCheck
updated 4 days ago by
GenoMax
150k • written 5 days ago by
KirGen
▴ 30
0
votes
0
replies
178
views
Comparing HMMER vs. HHrepID for LRR Repeat Detection and Boundary Consistency
hmmer
repeats
4 days ago by
jllPons
• 0
0
votes
0
replies
215
views
circos plot help
visualization
SNV
genomics
circos
updated 3 days ago by
Ram
45k • written 5 days ago by
Genomancer
• 0
2
votes
3
replies
318
views
DAVID List Upload/Gene Conversion Tool
DAVID
updated 4 days ago by
Ram
45k • written 5 days ago by
b5708137
• 0
0
votes
8
replies
3.0k
views
6 follow
CIBERSORTx error: 'x' must be an array of at least two dimensions
matrix
CIBERSORTx
signature
updated 5 days ago by
GenoMax
150k • written 2.7 years ago by
Jie
• 0
1
vote
2
replies
588
views
Can I combine segment results from Sequenza and cnvkit?
CNV
sequenza
cnvkit
5 days ago by
Ram
45k
1
vote
6
replies
461
views
Shotgun dataset with polyG, low qualiity
shotgun-data
updated 3 days ago by
andres.firrincieli
3.9k • written 5 days ago by
shevch2009
• 0
0
votes
2
replies
287
views
MAGeCK: Doing two sided test on gene level?
MAGeCK
5 days ago by
gernophil
▴ 120
0
votes
5
replies
395
views
Is TETranscripts useful for repetitive sequences analysis?
TEtranscripts
updated 4 days ago by
Michael
55k • written 5 days ago by
frarodmar17
• 0
2
votes
5
replies
398
views
SlingShot and Subsetting data
scrna
slingshot
trajectory
updated 3 days ago by
jared.andrews07
★ 18k • written 5 days ago by
carolofharvest
▴ 50
0
votes
1
reply
382
views
Bulk searching UniProt
uniprot
updated 5 days ago by
Elisabeth Gasteiger
★ 2.4k • written 9 days ago by
timothy.kirkwood
▴ 140
4
votes
6
replies
420
views
Problem with Accession Number Changes in UniProt FASTA Sequences
FASTA
Accession
Uniprot
IdMapping
4 days ago by
bioinfo_enthusiast
• 0
1
vote
2
replies
427
views
PPI Network Analysis of Virulence Genes in Morganella morganii Using STRING Database
PPI
STRING
5 days ago by
bioinfo_enthusiast
• 0
15
votes
12
replies
814
views
7 follow
Forum:
Reproducibility Crisis
R-Bioinformatics
updated 3 days ago by
i.sudbery
21k • written 6 days ago by
ParastooA
▴ 20
6
votes
13
replies
7.5k
views
7 follow
Getting sample information from GEO
GEO
NCBI
updated 5 days ago by
DareDevil
★ 4.4k • written 7.9 years ago by
Tom_L
▴ 360
0
votes
3
replies
317
views
How to Close a Phage Genome? Issues with PhageTerm and CheckV Completeness
phage
genome
assembly
PhageTerm
updated 5 days ago by
GenoMax
150k • written 5 days ago by
mail2steff
▴ 70
120,848 results • Page
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Variant Generation Using Longshot
A rust binding for pairwise/multiple sequence aligner: bsalign-rs
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Answer: Understanding Re-use of Query Sequences in Long Read Alignments
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Comment: SlingShot and Subsetting data
Reproducibility Crisis
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Comment: Depth in Cram file does not match depth in VCF file
by
karl.stamm
4.1k
Who made the VCF file? samtools also will downsample during genotype calling. In this case, I see it reports allele depths of 4 and 2, and…
Comment: Depth in Cram file does not match depth in VCF file
by
shu8
• 0
Hi, Thank you for answering, and I have tried to follow your instruction to turn the downsampling off in preference, but they are still d…
Comment: Depth in Cram file does not match depth in VCF file
by
GenoMax
150k
Guess you forgot to attach the image. You can edit the post above and add that. IGV may down sample data when displaying it so make sure y…
Answer: Should I process two complete sets of 10x single-cell multiomics sequencing file
by
GenoMax
150k
Files included in this link are technical replicates from lanes 1 through 4 and have the same `S21` number: https://www.encodeproject.org/e…
Comment: Should I process two complete sets of 10x single-cell multiomics sequencing file
by
Wu-Sheng Zhang
• 0
Hi @genomax , thank you very much! So, if this is just technical replicates, does it mean I can reasoablely "merge" S7 and S31 and them pro…
Comment: Should I process two complete sets of 10x single-cell multiomics sequencing file
by
GenoMax
150k
It is a little confusing since the same sample can't be included in two rows when demultiplexing the data using `bcl-convert` (which leads …
Comment: How to filter Hmmsearch alignment
by
Mensur Dlakic
★ 29k
I don't know how to help with your main question, as this is an unusual approach. You will probably have to write a custom script. Before y…
Comment: Perform DEGs with pyDESeq2 in CCLE Melanoma Data But Contains Negative Values
by
mete.han.celebi
• 0
Thank you so much for your reply! I will check it now!
Answer: Perform DEGs with pyDESeq2 in CCLE Melanoma Data But Contains Negative Values
by
ATpoint
87k
> negative values for some genes in this CCLE melanoma data. I think it arises since CCLE data is a log2 transformed Nobody can tell you…
Comment: How to concatenate different domains in the target database identified by hmmsea
by
GenoMax
150k
See the answer here as an option -->https://www.biostars.org/p/446822/
Answer: Defining residues as buried or exposed based in ASAs/RSAs
by
Dan A
• 0
I was also interested in this topic recently. What I've tried to do is to fit a 2 component Gaussian mixture model to an array of SASA valu…
Answer: Understanding Re-use of Query Sequences in Long Read Alignments
by
LauferVA
4.6k
@charles , You're right to wonder - even a very thoughtful approach, like yours, will generate some confusion. I'll indicate some "clues" …
Comment: Associating VDJ clonotyping data with scRNA-seq in Seurat
by
garcesj
▴ 50
It's a great workaround. My only question is about just removing the duplicates (`tcr <- tcr[!duplicated(tcr$barcode), ]`). Aren't we losin…
Comment: Discrepancy between BAM and vcf
by
Istvan Albert
102k
I will also say that if you take any variant caller and then look at the corresponding BAM file, you'll find many minor inconsistencies - i…
Comment: Lift over of GWAS summary stat file from Hg38 to Hg19
by
Mllepnos
• 0
Thanks a lot for the recommendation to use bcftools +munge and +liftover instead of UCSC liftOver — I’ll definitely try that!
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