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116,882 results • Page
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News:
Online course: An Introduction to Nanopore Direct RNA Sequencing
Nanopore
RNAseq
1 hour ago by
carlopecoraro2
★ 2.5k
0
votes
1
reply
123
views
input file in rmats
rmats
updated 3 hours ago by
Mathew
▴ 90 • written 2 days ago by
Lambodarswain316
• 0
0
votes
1
reply
144
views
Kraken2 database
kraken
microbialdb
database
krakendb
kraken2
updated 10 hours ago by
Mathew
▴ 90 • written 1 day ago by
Christopher
• 0
6
votes
6
replies
167
views
Longest transcript variant per gene
transcript
longest
variant
orthofinder
updated 5 hours ago by
Mathew
▴ 90 • written 10 hours ago by
sansan_96
▴ 90
2
votes
2
replies
127
views
error in fun(x((i)), ...) : only defined on a data frame with all numeric alike variables
studio
Cibersort
R
updated 11 hours ago by
Mathew
▴ 90 • written 14 hours ago by
Azra
▴ 10
795
votes
167
replies
143k
views
109 follow
News:
The Biostar Handbook. A bioinformatics e-book for beginners.
training
handbook
updated 3 months ago by
Biostar
2.7k • written 7.4 years ago by
Istvan Albert
100k
2
votes
1
reply
142
views
Failed to open VCF file
GATK
sentieon
BWA-MEM
updated 20 hours ago by
Pierre Lindenbaum
161k • written 1 day ago by
melissachua90
▴ 70
9
votes
7
replies
7.1k
views
Align paired and unpaired reads simultaneously using Bowtie2?
alignment
updated 20 hours ago by
Ruqaiya
• 0 • written 5.7 years ago by
xiaozhongzhiping
▴ 20
0
votes
1
reply
140
views
Adata.raw.X in LIANA, something wrong with conversion from Seurat to adata in python.
k
updated 12 hours ago by
fracarb8
★ 1.6k • written 21 hours ago by
beginner123
• 0
6
votes
4
replies
12k
views
Trimmomatic: What is the difference between paired and unpaired output files in paired-end mode
trimmomatic
paired-end
updated 21 hours ago by
Ruqaiya
• 0 • written 6.4 years ago by
dllopezr
▴ 130
0
votes
0
replies
72
views
imputation through beagle
panel
beagle
reference
imputation
22 hours ago by
analyst
▴ 50
0
votes
1
reply
109
views
java.nio.bufferunderflowexception haplotypecaller error for bqsr reads
deducplicated
java.nio.bufferunderflowexception
haplotypecaller
bqsr
updated 20 hours ago by
Pierre Lindenbaum
161k • written 22 hours ago by
analyst
▴ 50
0
votes
4
replies
233
views
Is it Possible to "Merge" data from Replicates within a VCF SNP File
snp
vcf
plink
bioinformatics
genomics
13 hours ago by
ajbarrett98
• 0
0
votes
10
replies
350
views
In IGV is this a heterogeneous mutation or false call?
mutations
IGV
heterogeneous
updated 1 day ago by
swbarnes2
14k • written 1 day ago by
Tuck898
• 0
1
vote
3
replies
175
views
Tassel 5 GBS: Is there something wrong with my fastqs?
tassel
fastq
gbs
updated 1 day ago by
GenoMax
142k • written 1 day ago by
meck
• 0
3
votes
3
replies
183
views
what is another word for a BLAST "hit"?
blast
alignment
1 day ago by
dec986
▴ 380
1
vote
2
replies
176
views
Genome Assembly task + Protein Translation, assignment advice on a question
sequence-analysis
protein-synthesis
22 hours ago by
rackbersingh
• 0
0
votes
1
reply
133
views
extract viral protein of interest from 10k whole viral genomes
nBLAST
viral-genome
updated 1 day ago by
Ram
43k • written 1 day ago by
Shwetha
• 0
0
votes
0
replies
99
views
Practical Haplotype Graph v2 not finding correct paths
Pangenome
PHG
graph
1 day ago by
beantkapoor16
• 0
0
votes
0
replies
101
views
Marker Features variance by cluster, sample, and treatment group
Seurat
scATAC-seq
ArchR
updated 1 day ago by
Ram
43k • written 1 day ago by
naomiboldon
• 0
1
vote
3
replies
202
views
How to format "I" and "D" in vcf version 4.2 for liftover analysis in GATK
gatk
vcf
liftover
updated 1 day ago by
Ram
43k • written 1 day ago by
Omics data mining
▴ 260
9
votes
6
replies
12k
views
samtools tview symbols
samtools
updated 8.8 years ago by
Ashutosh Pandey
12k • written 8.8 years ago by
biolab
★ 1.4k
1
vote
7
replies
514
views
Filtering Multi-sample VCF file for all except one Genotype
variant
SNP
VCF
updated 1 day ago by
Pierre Lindenbaum
161k • written 4 days ago by
schmince
• 0
0
votes
5
replies
228
views
Too many unpaired forward reads found by Trimmomatic
Trimmomatic
1 day ago by
SilhouetteQ
• 0
0
votes
1
reply
125
views
Alignment of samples with spike-in
alignment
multimapping
RNA-seq
ChIP-seq
spike-in
updated 1 day ago by
GenoMax
142k • written 1 day ago by
maria.soler
• 0
0
votes
2
replies
212
views
How are score_weights calculated in this code?
single-cell
22 hours ago by
carolofharvest
▴ 40
0
votes
1
reply
163
views
How to convert Haps file to vcf file?
pre-phasing
GWAS
imputation
updated 1 day ago by
curious
▴ 750 • written 1 day ago by
SeoGyun
• 0
2
votes
12
replies
2.7k
views
6 follow
CNVKIT - unable to produce scatter and diagram pdfs
cnvkit
updated 4 days ago by
Anitha
• 0 • written 4.8 years ago by
ww22runner
▴ 60
0
votes
0
replies
106
views
Trouble converting tfam and tped to map and ped files
plink
ped
tfam
tped
map
2 days ago by
Samantha
• 0
0
votes
1
reply
138
views
Microbial Signal Transduction Database
MiST
updated 1 day ago by
zx8754
11k • written 2 days ago by
Shravani
• 0
0
votes
1
reply
150
views
DESeq2 error
DESeq2
updated 2 days ago by
ATpoint
82k • written 2 days ago by
sooni
▴ 20
0
votes
0
replies
98
views
Allele specific expression of imprinted gens from 10x scRNA-seq data
scrna-seq
imprinted
10x
genes
2 days ago by
singcell
• 0
0
votes
1
reply
160
views
When should I use R-MarkDown over R-Script ?
r
rscript
rmarkdown
updated 2 days ago by
ATpoint
82k • written 2 days ago by
Amr
▴ 160
0
votes
2
replies
169
views
LncRNA Nomenclature
ENST
nomenclature
lncrna
GBB
ENSG
2 days ago by
jain72744
▴ 10
0
votes
0
replies
103
views
Nomalization - TCGA, RNA-seq and Microarray
TCGA
RNA-seq
Nomalization
Microarray
2 days ago by
jain72744
▴ 10
6
votes
2
replies
173
views
EdgeR - relationship between logFC and coefficients
differential-expression
r
edger
updated 2 days ago by
Gordon Smyth
★ 7.1k • written 2 days ago by
gBioStar5
▴ 10
2
votes
5
replies
330
views
Importing a fastq file
Fastq
updated 2 days ago by
size_t
▴ 120 • written 3 days ago by
oumo
• 0
3
votes
1
reply
145
views
Question about methylation location
Methylation
WGBS
bisulfide
updated 1 day ago by
dthorbur
★ 1.9k • written 2 days ago by
Eren
• 0
0
votes
0
replies
110
views
Krona Pie-chart taxanomy IDs were not found warning. Taxonomy Classification Metagenomics
Classification
Metagenomics
Krona
Kraken2
2 days ago by
Aytaç
• 0
0
votes
0
replies
124
views
How do I calculate SE or P value if I only have BETA
prscsx
beta
se
pvalue
updated 1 day ago by
zx8754
11k • written 2 days ago by
curious_butterfly
• 0
0
votes
0
replies
118
views
supervised admixture
supervised
admixture
2 days ago by
RT
▴ 10
0
votes
0
replies
119
views
Two-Sample Mendelian Randomization: Association between Instrumental Variable and Outcome
Randomization
Mendelian
two-sample
2 days ago by
Nikki
• 0
2
votes
0
replies
120
views
News:
course on Landscape Genomics at the EPFL in Lausanne (June 17-21)
LandscapeGenomics
SNPs
LocalAdaptation
GIS
2 days ago by
carlopecoraro2
★ 2.5k
0
votes
8
replies
373
views
Different output for read length
samtools
BAM
2 days ago by
marco.barr
▴ 100
0
votes
1
reply
339
views
Snakemake fails to find conda in PBS
snakemake
updated 2 days ago by
tim.booth
▴ 60 • written 29 days ago by
yixinzeng
• 0
0
votes
2
replies
195
views
Presence of unknown sites in ANNOVAR output file
ANNOVAR
updated 1 day ago by
Ram
43k • written 2 days ago by
sainavyav22
• 0
3
votes
4
replies
274
views
Truncated metadata file report from ENA Portal API
ena
python
1 day ago by
Giulia
• 0
0
votes
0
replies
159
views
What is workflow for de-novo assembling of nuclear and mito genomes of non-model organisms
de-novo
WGS
DNA-seq
assembling
2 days ago by
Matvii Mykhailichenko
• 0
0
votes
3
replies
536
views
JASPAR2024_getMatrixSet error
JASPAR2024
getMatrixSet
updated 2 days ago by
Ram
43k • written 11 weeks ago by
maplewj
▴ 10
0
votes
3
replies
226
views
How to convert normalized BigWig file to count matrix?
count-matrix
BigWig
updated 2 days ago by
Ram
43k • written 2 days ago by
feather-W
• 0
116,882 results • Page
1 of 2338
Recent Votes
Comment: Longest transcript variant per gene
Comment: Longest transcript variant per gene
Answer: Longest transcript variant per gene
Answer: Longest transcript variant per gene
Comment: Longest transcript variant per gene
Comment: Longest transcript variant per gene
Answer: install package
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Recent Replies
Answer: input file in rmats
by
Mathew
▴ 90
Hi, In the example they give in their GitHub (https://github.com/Xinglab/rmats-turbo/blob/v4.3.0/README.md): They have 2 sample groups wi…
Comment: Longest transcript variant per gene
by
Mathew
▴ 90
I'm glad it worked well for you! Good luck with the rest of your project. I wish you the best.
Comment: Longest transcript variant per gene
by
sansan_96
▴ 90
Thanks so much
Comment: Longest transcript variant per gene
by
sansan_96
▴ 90
Hello again, It works very well, thank you very much for this solution.
Comment: Longest transcript variant per gene
by
sansan_96
▴ 90
Hello Mathew, Thanks for your answer, I'll try it and come back.
Answer: Longest transcript variant per gene
by
Mathew
▴ 90
Hi, why not write code to extract the longest variant? I copied these two in a txt file called "input.txt", and made three dummy variants …
Comment: Longest transcript variant per gene
by
GenoMax
142k
https://www.biostars.org/p/107759/<br> https://www.biostars.org/p/403649/ <!-- this is it -->
Answer: Kraken2 database
by
Mathew
▴ 90
Sorry, what analysis are you trying to perform with these databases? Based on your question, it appears you are using Kraken2 and Bracken.…
Comment: error in fun(x((i)), ...) : only defined on a data frame with all numeric alike
by
Mathew
▴ 90
I looked up a publication using CIBERSORT to see how they got the package, and indeed they acquired it through official website application…
Comment: Adata.raw.X in LIANA, something wrong with conversion from Seurat to adata in py
by
fracarb8
★ 1.6k
If you are using R, you should check the liana R implementation (https://github.com/saezlab/liana).
Comment: Is it Possible to "Merge" data from Replicates within a VCF SNP File
by
ajbarrett98
• 0
Thank you Pierre, I am going to take some time to get my head around this and report back if it works.
Comment: Is it Possible to "Merge" data from Replicates within a VCF SNP File
by
ajbarrett98
• 0
Thanks for the crosspost! Just trying to get things figured out.
Answer: error in fun(x((i)), ...) : only defined on a data frame with all numeric alike
by
ATpoint
82k
To the best of my knowledge, CIBERSORT is and has always and only been available via the official website application from Stanford. Whatev…
Comment: BioLabDonkey - new Mac program for molecular biologists
by
vytarasov
▴ 180
Update of BioLabDonkey - Version 5.6 - In silico PCR function is added.
Comment: Is it Possible to "Merge" data from Replicates within a VCF SNP File
by
Pierre Lindenbaum
161k
cross posted: https://stackoverflow.com/questions/78462732/ > Please mind that posting the same question to multiple sites can be perceive…
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