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121,903 results • Page
619 of 2439
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Votes
Replies
0
votes
0
replies
947
views
How do I predict HLA's haplotype from WES data?
HLA
WES
haplotype
4.2 years ago by
kwanghoon
▴ 20
0
votes
3
replies
2.0k
views
fgsea gene names
fgsea
updated 4.2 years ago by
Kevin Blighe
89k • written 4.2 years ago by
barix
▴ 20
0
votes
1
reply
1.3k
views
CPC2.py can not work
CPC2
updated 4.2 years ago by
Nitin Narwade
★ 1.7k • written 4.2 years ago by
17318598206
▴ 30
4
votes
1
reply
1.5k
views
Does normalization in edgeR conflict with tximeta-generated offset matrix?
Normalization
tximeta
RNA-Seq
edgeR
updated 4.2 years ago by
ATpoint
89k • written 4.2 years ago by
skjw1029
▴ 80
4
votes
11
replies
3.1k
views
How to find the fasta file with maxium number of amino acids?
protein
fasta
sequence
4.2 years ago by
shahbaz.ahmed
▴ 40
0
votes
0
replies
543
views
can we subdivide a single .fa file having cds, cdna, protein and genomic sequence in to separate file having only one type of sequence?
bioconductor
updated 4.2 years ago by
Ram
45k • written 4.2 years ago by
shahbaz.ahmed
▴ 40
3
votes
3
replies
1.2k
views
Ngs : how check if two samples come frome the same family?
exome
family
Genome
updated 4.2 years ago by
ATpoint
89k • written 4.2 years ago by
quentin54520
▴ 120
0
votes
2
replies
1.2k
views
program/ software to generate large synthetic benchmark gene/ protein interaction network
PPI
interaction
benchmark
network
R
4.2 years ago by
cwwong13
▴ 40
0
votes
0
replies
950
views
Job:
Bioinformatics position at NIOO-KNAW (Wageningen, The Netherlands)
python
snakemake
Linux
git
Netherlands
4.2 years ago by
m.dehollander
▴ 50
3
votes
1
reply
1.1k
views
identification of lncRNA
lncRNA
mRNA
RNA-seq
updated 4.2 years ago by
grant.hovhannisyan
★ 2.6k • written 4.2 years ago by
17318598206
▴ 30
6
votes
18
replies
6.8k
views
6 follow
How to generate a combined read count txt file with header as file name
bash
linux
awk
R
updated 4.1 years ago by
Rajesh
▴ 10 • written 6.0 years ago by
Bioinfonext
▴ 470
2
votes
4
replies
2.2k
views
whole genome sequence for origami 2 (DE3) and rosetta 2 (DE3)
ecoli
cells
rosetta2
origami2
competent
Novagen
updated 3.3 years ago by
Sonia
• 0 • written 4.2 years ago by
mittu1602
▴ 200
1
vote
2
replies
1.2k
views
Is geneontology.org down?
database
geneontology
4.2 years ago by
EagleEye
7.6k
3
votes
4
replies
1.6k
views
population stratification for candidate gene association study
stratification
candidate
population
PCA
gene
4.2 years ago by
putty
▴ 40
9
votes
9
replies
5.1k
views
6 follow
Forum:
Choose between AMD and INTEL Server CPU in 2021-2022
hardware
server
updated 4.2 years ago by
Jean-Karim Heriche
27k • written 4.2 years ago by
JustinZhang
▴ 140
0
votes
0
replies
1.2k
views
HiC matrix in .txt format to .h5
matrix
HiC
h5
txt
4.2 years ago by
Oleczkaff
• 0
2
votes
2
replies
1.2k
views
Genotype imputation - do SNP IDs of input files and reference panels matter?
genotype
SNP
reference
VCF
imputation
updated 4.2 years ago by
4galaxy77
2.9k • written 4.2 years ago by
Volka
▴ 180
2
votes
1
reply
1.4k
views
Why am I getting microRNA genes from a 10X genomics dataset?
RNA-seq
microRNA
4.2 years ago by
Gene_MMP8
▴ 240
1
vote
0
replies
1.2k
views
QIIME2 quality control
control
dada2
quality
qiime2
4.2 years ago by
blur
▴ 280
0
votes
0
replies
1.7k
views
Job:
Postdoc – Natural Language Processing / Text Mining
NLP
PyTorch
Text
Mining
Tensorflow
4.2 years ago by
info
▴ 80
2
votes
4
replies
1.6k
views
How to create gene level data from a probe level data?
R
sum
mean
gene
microarray
4.2 years ago by
mohammedtoufiq91
▴ 270
3
votes
4
replies
1.6k
views
DENOVO ASSEMBLY
assembly
NGS
Assembly
Denovo
updated 4.2 years ago by
Carambakaracho
★ 3.3k • written 4.2 years ago by
askari.arezou94
▴ 30
1
vote
4
replies
1.8k
views
SNP ID
SNP
ID
dbSNP_143
4.2 years ago by
shamsurrahaman132
▴ 10
1
vote
4
replies
6.7k
views
How to fix "ValueError: not enough values to unpack (expected 3, got 1)" when excuting batch analysis?
batch
germline cnv
updated 4.2 years ago by
rahul
• 0 • written 5.1 years ago by
mychung3265
• 0
4
votes
4
replies
1.3k
views
What is the difference between Assignment and Prediction?
protein
protein-structure
protein-structure-prediction
updated 4.2 years ago by
Mensur Dlakic
★ 30k • written 4.2 years ago by
user366312
▴ 20
0
votes
5
replies
1.8k
views
CNVkit Feedback about panel or normales needed
CNVkit
4.2 years ago by
mphoeppner
• 0
2
votes
0
replies
687
views
panelcn.mops package to build up control.bam file
panelcn.mops
samtools
4.2 years ago by
jimmy0958073736
▴ 40
1
vote
3
replies
1.2k
views
Blast results processing lines bigger than 60
blast
unix
commands
awk
result
4.2 years ago by
hdtms
▴ 20
0
votes
14
replies
2.6k
views
error relate to R
TWAS
SNP
R
updated 4.2 years ago by
Kevin Blighe
89k • written 4.2 years ago by
rheab1230
▴ 150
1
vote
0
replies
1.1k
views
DepthPerSampleHC and StrandBiasBySample HaplotypeCaller Warnings in GATK
Haplotypecaller
4.2 years ago by
Jianing
▴ 10
2
votes
0
replies
633
views
scRNA-seq datasets for different cell lines
scRNAseq
4.2 years ago by
Alexander
▴ 220
2
votes
9
replies
3.2k
views
Getting command line blastn results for the complementary strand
blast
command-line
blastn
updated 4.2 years ago by
lieven.sterck
15k • written 4.2 years ago by
langziv
▴ 70
2
votes
2
replies
1.2k
views
Differentially gene expression multispecies
Gene
Expression
Multiespecies
RNAseq
4.1 years ago by
tiagobellintani
▴ 40
3
votes
2
replies
1.3k
views
Differentially gene expression analysis using limma
Limma
packages
updated 4.2 years ago by
Hamid Ghaedi
3.3k • written 4.2 years ago by
fahim
▴ 20
2
votes
5
replies
2.6k
views
Weird characters in yeast reference gff3
SGD
gff3
yeast
gff
4.2 years ago by
liorglic
★ 1.5k
7
votes
3
replies
1.8k
views
How to normalize and transform RNA-seq data of different samples for PCA?
TMM
PCA
RNA-seq
edgeR
updated 4.2 years ago by
Kevin Blighe
89k • written 4.2 years ago by
Pratik
★ 1.1k
0
votes
2
replies
2.2k
views
Manhattan plot p-value
manhattan
plot
snp
4.2 years ago by
shamsurrahaman132
▴ 10
0
votes
0
replies
642
views
IGV add contig/chr to genome file within session
genome
IGV
bam
alignment
4.2 years ago by
noodle
▴ 650
0
votes
1
reply
1.1k
views
Which error bar to use to show gene expression from single-cell RNAseq data
expression
rnaseq
statistics
gene
single-cell
4.2 years ago by
gundalav
▴ 380
0
votes
0
replies
1.7k
views
Generating comprehensive data for Promethease and Codegen.eu from WGS
WGS
gVCF
Promethease
raw
calling
variant
4.2 years ago by
Tim
• 0
0
votes
0
replies
679
views
rsem-calculate-expression error
RNA-Seq
rsem
rsem-calculate-expression
4.2 years ago by
Bhoomika
• 0
3
votes
4
replies
1.4k
views
How to calculate the distribution of histone modifications on transcription factors
modifications
histone
4.2 years ago by
koyee_d
▴ 20
2
votes
2
replies
2.5k
views
How to convert genotypes "1, 2" to "0,1, 2"?
snp
plink
updated 2.0 years ago by
karthick
▴ 10 • written 4.2 years ago by
Star:)
▴ 50
0
votes
2
replies
910
views
Extracting coding region for multiple sequences.
Coding
Region
4.2 years ago by
QAZ
▴ 20
2
votes
8
replies
4.8k
views
Trying to run FIMO from Meme suite using command line
meme
motif
updated 4.2 years ago by
seidel
11k • written 4.2 years ago by
DormoD
• 0
3
votes
3
replies
1.1k
views
How to identify and characterize novel genes?
Novel
updated 4.2 years ago by
MSRS
▴ 590 • written 4.2 years ago by
micahadekunle
• 0
0
votes
0
replies
659
views
How was hierarchical clustering established for mRNA expression data?
clustering
mRNA
expression
4.2 years ago by
ceruleanivy
▴ 50
0
votes
1
reply
1.1k
views
Help with processing GSE63060: Illumina data that does not have lumi requirements
lumi
illumina
Bioconductor
R
updated 4.2 years ago by
Kevin Blighe
89k • written 4.2 years ago by
mincej20
• 0
1
vote
1
reply
1.1k
views
Minimum coverage for structural variant calling
variant
structural
coverage
updated 4.2 years ago by
Zhilong Jia
★ 2.2k • written 4.2 years ago by
5utr
▴ 370
11
votes
10
replies
12k
views
7 follow
How To Calculate Genetic Heterogeneity From Genotype Data - How Useful Is This Measure?
genetics
snp
genotyping
updated 3.5 years ago by
Ram
45k • written 14.6 years ago by
Larry_Parnell
16k
121,903 results • Page
619 of 2439
Recent Votes
Answer: Tried building a compact sequence format with 4-bit storage
Tried building a compact sequence format with 4-bit storage
Shift in RNA 3' position, Term-Seq vs RNASeq
Comment: STARlong for pacbio Isoseq reads
Comment: Automatically annotating a feature using a genbank file
Answer: Is this PCA plot correct??
Answer: Is this PCA plot correct??
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Comment: Is total miRNA in EV constant? Implications for library size normalization.
by
Gordon Smyth
★ 8.3k
RNA-seq is very good at relative analyes. It would be straightforward to determine which miRNAs are relatively more abundant, compared to o…
Comment: Tried building a compact sequence format with 4-bit storage
by
Pranava
▴ 10
Woah!!! Thank you very much, Matthias. I honestly didn't even know some of those existed and I will definitely go through them and try to u…
Answer: Tried building a compact sequence format with 4-bit storage
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Matthias Zepper
5.1k
Hello Pranava, Thanks for sharing your repository. Devising a new file format is an interesting undertaking and certainly a task with many…
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`LOC` gene ID's are often assigned to uncharacterized genes and you may not get useful information from databases for them, thus they will …
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piffelpaff
• 0
Sorry to revive this ancient thread but I'm currently discussing the same question with some people in my lab and would love to somebody po…
Answer: STARlong for pacbio Isoseq reads
by
YuZJ
• 0
Hello, you may try deSALT (DOI: 10.1186/s13059-019-1895-9, GitHub: ydLiu-HIT/deSALT) or uLTRA (DOI: 10.1093/bioinformatics/btab540, GitHub:…
Comment: Shift in RNA 3' position, Term-Seq vs RNASeq
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acvill
▴ 350
Without knowing the details of the Term-seq method, could the 38 nt shift be accounted for by the difference in the position of the ribosom…
Comment: STARlong for pacbio Isoseq reads
by
Buffo
★ 2.4k
Thanks, I'll give it a try.
Comment: STARlong for pacbio Isoseq reads
by
GenoMax
153k
You could give `mapPacBio.sh` from BBMap suite a try while you wait for other answers. That works for reads up to 6 kb. BBMap has a new hom…
Comment: STARlong for pacbio Isoseq reads
by
Buffo
★ 2.4k
The average is 1.8kb. I was planning to post it on GitHub, but it seems like the repository has been unattended for the last months, so I d…
Comment: Getting just fastqc.zip file?
by
GenoMax
153k
Yes, You can either use it on command line or use the graphical user interface.
Comment: STARlong for pacbio Isoseq reads
by
GenoMax
153k
What is the average length of your reads? That error sounds like a bug, so you may want to post that on `STAR` repo as an issue. I assume …
Comment: Getting just fastqc.zip file?
by
pourhangleila95
• 0
I want to perform fastQC on my data.Do you use fastQC software for doing it?
Comment: Whole Genome Sequencing IG regions
by
719
• 0
Sorry for the poor wording of the original post, also should say I really appreciate people taking a moment to look at my post. My main con…
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