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Showing :
questions
0
votes
2
replies
1.1k
views
How to bypass WGCNA installation error?
wgcna
microarray
R
3.9 years ago by
fernardo
▴ 170
12
votes
24
replies
5.8k
views
How to find p-value of the modules in WGCNA?
wgcna
microarray
RNA-Seq
R
updated 4.2 years ago by
149abhi
▴ 10 • written 6.1 years ago by
fernardo
▴ 170
2
votes
3
replies
2.5k
views
How to check if first two components of PCA are separated without visualisation?
pca
machine learning
R
Python
NGS
updated 5.1 years ago by
raunakms
★ 1.1k • written 5.1 years ago by
fernardo
▴ 170
3
votes
11
replies
2.1k
views
Can this PCA be a highly good result?
machine learning
PCA
RNA-seq
NGS
5.2 years ago by
fernardo
▴ 170
4
votes
22
replies
3.9k
views
Is it fine to run SVM on RNA-seq read counts?
RNA-Seq
SVM
machine learning
classification
5.2 years ago by
fernardo
▴ 170
6
votes
10
replies
2.3k
views
Why different DEGs between my result and the author's result?
limma
microarray
differential-gene-expression
updated 26 days ago by
Ram
43k • written 6.1 years ago by
fernardo
▴ 170
3
votes
4
replies
1.4k
views
How to copyright your script?
R
python
java
software
copyright
updated 7.5 years ago by
Farbod
★ 3.4k • written 7.5 years ago by
fernardo
▴ 170
10
votes
22
replies
3.6k
views
Can ncRNAs be found from all RNA-seq data?
RNA-Seq
deepBase
miRDeep2
ncRNA
updated 7.7 years ago by
Edalat
▴ 30 • written 8.1 years ago by
fernardo
▴ 170
4
votes
8
replies
2.8k
views
why is this example homozygous 0/0 ?
SNP
updated 8.1 years ago by
Jorge Amigo
14k • written 8.1 years ago by
fernardo
▴ 170
0
votes
6
replies
3.7k
views
When is recommended to remove or keep Unpaired "Orphan" reads in downstream analysis?
RNA-Seq
SNP
alignment
exome-seq
samtools
updated 2.9 years ago by
Devon Ryan
104k • written 8.1 years ago by
fernardo
▴ 170
20
votes
17
replies
11k
views
9 follow
Why GATK and bcftools SNP calling different?
SNP
next-gen
GATK
bcftools
variant calling
updated 24 months ago by
Kevin Blighe
87k • written 8.1 years ago by
fernardo
▴ 170
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