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58 results • Page
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Views
Votes
Replies
238
votes
176
replies
85k
views
73 follow
Tutorial:
Survival analysis of TCGA patients integrating gene expression (RNASeq) data
RNA-Seq
Survival
TCGA
updated 11 days ago by
Ram
39k • written 7.8 years ago by
TriS
★ 4.6k
78
votes
42
replies
29k
views
25 follow
Tutorial:
Extract Total Non-Overlapping Exon Length Per Gene With Bioconductor
fpkm
rna-seq
bioconductor
updated 27 days ago by
Ram
39k • written 9.6 years ago by
Irsan
★ 7.7k
83
votes
34
replies
16k
views
22 follow
Tutorial:
Enrichment Analysis, Clustering and Scoring with pathfindR
enrichment
R
pathway
active-subnetwork
updated 9 days ago by
adelheidkratzer
• 0 • written 5.0 years ago by
egeulgen
★ 1.3k
45
votes
28
replies
7.3k
views
9 follow
Tutorial:
How to Use Biostars, Part-I: Questions, Answers, Comments and Replies
documentation
meta
how-to
17 days ago by
Ram
39k
9
votes
23
replies
8.6k
views
7 follow
Tutorial:
OrthoMCL installation on Ubuntu Linux
ubuntu
orthomcl
mysql
linux
updated 17 days ago by
Ram
39k • written 5.4 years ago by
vimalkvn
▴ 310
59
votes
15
replies
12k
views
Tutorial:
Which human reference genome should I use?
assembly
genome
alignment
updated 10 days ago by
Ram
39k • written 4.7 years ago by
finswimmer
16k
17
votes
13
replies
1.7k
views
Tutorial:
Screen shots of text (please don't)!
meta
updated 24 days ago by
Ram
39k • written 6.2 years ago by
Michael
52k
12
votes
11
replies
6.7k
views
Tutorial:
How to upload your RNA-Seq data to NCBI Sequence Read Archive (SRA)
NCBI
Bioproject
SRA
BioSample
updated 25 days ago by
Ram
39k • written 6.2 years ago by
CandiceChuDVM
★ 2.4k
9
votes
9
replies
3.7k
views
Tutorial:
Determine % of reference genome covered by aligned SAM/BAM
reference-coverage
ngs
updated 19 days ago by
Ram
39k • written 5.7 years ago by
Kevin Blighe
85k
11
votes
7
replies
13k
views
Tutorial:
Removing rows with duplicate values based on 1 or more key values - linux awk
awk
linux
bash
updated 19 days ago by
Ram
39k • written 5.7 years ago by
Kevin Blighe
85k
11
votes
7
replies
7.3k
views
Tutorial:
ClusterProfiler A software for functional enrichment of differentially expressed genes- A tutorial
clusterProfiler
Software
rna-seq
updated 16 days ago by
Ram
39k • written 2.3 years ago by
Novogene
▴ 300
39
votes
6
replies
17k
views
Tutorial:
Creating chromosome karyotype plot with R and ggplot2
ggplot2
R
chromosome
karyotype
updated 19 days ago by
Ram
39k • written 5.8 years ago by
steve
★ 3.3k
9
votes
5
replies
2.0k
views
Tutorial:
What is new in samtools release 1.5 [Solstice Release] (21st June 2017)
samtools
updated 20 days ago by
Ram
39k • written 5.9 years ago by
Istvan Albert
98k
5
votes
5
replies
6.1k
views
Tutorial:
use firehose_get to download TCGA data
tcga
RNA-Seq
updated 18 days ago by
Ram
39k • written 5.6 years ago by
jmzeng1314
▴ 130
10
votes
4
replies
2.9k
views
Tutorial:
CorLevelPlot - Visualise correlation results, e.g., clinical parameter correlations
correlation
corlevelplot
updated 16 days ago by
Ram
39k • written 5.3 years ago by
Kevin Blighe
85k
3
votes
4
replies
3.4k
views
Tutorial:
Gene Set Enrichment Analysis on T-BioInfo
gene
RNA-Seq
updated 10 days ago by
Ram
39k • written 4.6 years ago by
elia.brodsky
▴ 340
1
vote
4
replies
3.0k
views
Tutorial:
Applying machine learning to NGS transcriptomic data
next-gen
RNA-Seq
updated 13 days ago by
Ram
39k • written 5.1 years ago by
elia.brodsky
▴ 340
3
votes
4
replies
4.0k
views
Tutorial:
gencore: a tool to reduce sequencing noises by generating consensus reads
consensus
OpenGene
sequencing-noise
updated 13 days ago by
Ram
39k • written 5.1 years ago by
chen
★ 2.4k
2
votes
3
replies
2.4k
views
Tutorial:
It's about the journey, and not the destination
R
network
updated 24 days ago by
Ram
39k • written 6.2 years ago by
theobroma22
★ 1.2k
3
votes
3
replies
7.9k
views
Tutorial:
High Speed Downloading of SRA, SAM and Fastq Files
fastq
sam
Aspera-Connect
sra
updated 17 days ago by
Ram
39k • written 5.4 years ago by
Wenhu_Cao
▴ 100
3
votes
2
replies
2.1k
views
Tutorial:
Continuing Education (Pipelines): Best blogs, Online Lectures, Workshops, etc..
conferences
Workshops
updated 23 days ago by
Ram
39k • written 6.1 years ago by
jnowacki
▴ 100
10
votes
2
replies
3.4k
views
Tutorial:
Graph visualization with igraph in R
Visualization
igraph
Graph
R
Network
updated 24 days ago by
Ram
39k • written 6.2 years ago by
Jean-Karim Heriche
26k
7
votes
2
replies
1.7k
views
Tutorial:
Introduction to Human Genomics for Clinical Informaticists
genome
updated 19 days ago by
Ram
39k • written 5.8 years ago by
bdolin
▴ 90
18
votes
2
replies
5.5k
views
Tutorial:
Update kraken databases
database
kraken
k-mer
python
updated 23 days ago by
Ram
39k • written 6.1 years ago by
Sej Modha
5.2k
3
votes
2
replies
3.5k
views
Tutorial:
Galaxy Tutorial on ChIP-seq
galaxy
ChIP-Seq
updated 24 days ago by
Ram
39k • written 6.2 years ago by
anton
▴ 30
6
votes
2
replies
3.7k
views
Tutorial:
GATK method for filtering vcf lines using GT values at all or multisample level.
genome
vcf
genotype
variant-filtration
updated 23 days ago by
Ram
39k • written 6.0 years ago by
kirannbishwa01
★ 1.5k
5
votes
2
replies
2.8k
views
Tutorial:
Get GC Content from UCSC with perl script (mysql)
myql
ucsc
gc-content
perl
updated 24 days ago by
Ram
39k • written 6.1 years ago by
Shicheng Guo
★ 9.3k
20
votes
2
replies
7.2k
views
Tutorial:
Creating a karyotype plot with genes using karyoploteR
karyoploteR
visualization
R
genome
updated 18 days ago by
Ram
39k • written 5.5 years ago by
bernatgel
★ 3.4k
2
votes
2
replies
7.8k
views
Tutorial:
Use fastp to preprocess FASTQ data with unique molecular identifer (UMI) integrated
FASTQ
UMI
fastp
updated 18 days ago by
Ram
39k • written 5.5 years ago by
chen
★ 2.4k
11
votes
2
replies
7.4k
views
Tutorial:
Plotting the coverage and depth (Y-axis) statistics of a bam file along the genome (X-axis), using Samtools, awk and R.
genome
plot
coverage
samtools
updated 24 days ago by
Ram
39k • written 6.2 years ago by
kirannbishwa01
★ 1.5k
19
votes
2
replies
3.1k
views
Tutorial:
Beginner's Handbook to Next Generation Sequencing
NGS
updated 24 days ago by
Ram
39k • written 6.2 years ago by
support
▴ 640
3
votes
1
reply
2.1k
views
Tutorial:
Convert bam files to fastq in numbers as indicated in samtools flagstat stats.
samtools
bam
alignment
fastq
sequence
updated 23 days ago by
Ram
39k • written 6.0 years ago by
kirannbishwa01
★ 1.5k
0
votes
1
reply
2.8k
views
Tutorial:
Accessing sequences using batch entrez
genome
updated 18 days ago by
Ram
39k • written 5.6 years ago by
mawia.martha
• 0
10
votes
1
reply
7.7k
views
Tutorial:
How to select reads with specific flag using samtools
next-gen-sequencing
updated 19 days ago by
Ram
39k • written 5.7 years ago by
imlituan
▴ 110
7
votes
1
reply
2.0k
views
Tutorial:
A gentle introduction to biogo
sequence
golang
biogo
updated 18 days ago by
Ram
39k • written 5.6 years ago by
Botond Sipos
★ 1.7k
4
votes
1
reply
1.7k
views
Tutorial:
One of the easy way to achieve read count and RPKM file
RNA-Seq
updated 19 days ago by
Ram
39k • written 5.8 years ago by
maleknias
▴ 40
0
votes
1
reply
1.7k
views
Tutorial:
Nonparametric Regression STATA 15
STATA-15
Nonparametric-Regression
STATA
updated 17 days ago by
Ram
39k • written 5.4 years ago by
helgasaraswati
▴ 10
15
votes
1
reply
6.4k
views
Tutorial:
A compilation of conversion tools for BED, SAM/BAM, psl, pslx, blast tabular and blast xml
psl
SAM
blast
BED
updated 18 days ago by
Ram
39k • written 5.6 years ago by
Joseph Hughes
★ 3.0k
0
votes
0
replies
7.6k
views
Tutorial:
Multicollinearity VIF (Variance Inflation Factor) Analysis in Panel data EVIEWS 9
R
eviews
updated 17 days ago by
Ram
39k • written 5.4 years ago by
helgasaraswati
▴ 10
1
vote
0
replies
1.8k
views
Tutorial:
How to display Agilent CGH array in IGV
IGV
CGH
updated 18 days ago by
Ram
39k • written 5.5 years ago by
sacha
★ 2.4k
0
votes
0
replies
1.1k
views
Tutorial:
In the cloud - Guide to running VerifyBamID to estimate DNA sample contamination
sequence
cloud
dna
sequencing
updated 11 days ago by
Ram
39k • written 4.8 years ago by
corlinp
• 0
0
votes
0
replies
2.6k
views
Tutorial:
Autocorrelation With Breusch Godfrey Serial Correlation LM Test R Commander
LM-Test
R
Autocorrelation
Breusch-Godfrey
updated 17 days ago by
Ram
39k • written 5.5 years ago by
helgasaraswati
▴ 10
2
votes
0
replies
6.5k
views
Tutorial:
How to - Install Python packages in a virtual environment (virtualenv)
ubuntu
cutadapt
virtualenv
python
windows
updated 17 days ago by
Ram
39k • written 5.5 years ago by
vimalkvn
▴ 310
0
votes
0
replies
2.0k
views
Tutorial:
Transforming (Transformation) Data LN, Log, SQRT In R Commander
R
updated 17 days ago by
Ram
39k • written 5.4 years ago by
helgasaraswati
▴ 10
1
vote
0
replies
1.3k
views
Tutorial:
Fall 2017 Introduction to Human Genomics for Clinical Informaticists
genome
updated 17 days ago by
Ram
39k • written 5.4 years ago by
bdolin
▴ 90
4
votes
0
replies
2.1k
views
Tutorial:
Accurate prediction of active enhancers using PARE
ChIP-Seq
histone-modification
enhancer
updated 24 days ago by
Ram
39k • written 6.1 years ago by
Sachin Pundhir
▴ 100
3
votes
0
replies
2.1k
views
Tutorial:
Deep Learning for Cancer Immunotherapy
keras
tensorflow
updated 17 days ago by
Ram
39k • written 5.3 years ago by
Jeremy Leipzig
21k
0
votes
0
replies
1.2k
views
Tutorial:
Data Panel In R Commander
R
updated 17 days ago by
Ram
39k • written 5.5 years ago by
helgasaraswati
▴ 10
0
votes
0
replies
3.4k
views
Tutorial:
SFA (Stochastic Frontier Analysis) STATA 14
R
updated 17 days ago by
Ram
39k • written 5.3 years ago by
helgasaraswati
▴ 10
2
votes
0
replies
1.2k
views
Tutorial:
Free Book : Computational Biology of a cell signalling pathway using R
cell-signalling
R
Computational-Biology
updated 4 days ago by
Ram
39k • written 17 months ago by
sinha.shriprakash
▴ 20
58 results • Page
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Answer: How To Predict Pseudogenes In A Genome
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Comment: How to calculate TPM from featureCounts output
by
rpolicastro
12k
If you want to go that route, yes.
Comment: Difference between USCS exon coordinates and ensembl
by
ATpoint
72k
What did you download from UCSC? 1-off usually means one file is zero-based and the other 1-based. BED files from UCSC are 0-based, Ensembl…
Comment: Alignment of case vs. control from different origin
by
sativus
• 0
Thank you kindly for the explanation, it is highly appreciated. I suppose i was a bit confused as you quite often see people validating the…
Answer: Gene enrichment analysis
by
nux
▴ 10
Hello. For this you have to select 'hyper' as your method and then provide a complete list of genes which both include the candidate and no…
Comment: CNNScoreVariants Error
by
bestone
▴ 10
Thank you for replying I updated it worked but it gives another Error A USER ERROR has occurred: Invalid argument ' -V'.
Comment: Impute haplotypes (ImputePipelinePlugin) execution error - PHG
by
jrodrigu
• 0
Thank you so much. I made the suggested changes. However, I still have the same problem. Please check the new log file. https://github.c…
Comment: Getting same value for start and end position, "DNA methylation"
by
ATpoint
72k
That's a comment, not an answer, please use `ADD COMMENT`.
Comment: Getting same value for start and end position, "DNA methylation"
by
bioinfo_ga
▴ 50
Are you working on bisulphite kind of data or chipseq ????
Answer: How to calculate TPM from featureCounts output
by
bioinfo_ga
▴ 50
hi , You can use a python package rnanorm [https://pypi.org/project/rnanorm/]. The input required are your read count values from feature …
Comment: How to split a scRNA reads BAM or FASTQ file to a separate file for each cell by
by
biofalconch
▴ 580
Hey, if you arelady have the barcodes, you could use samtools `samtools view -h -b -f CB:Z:TAAGAGATCCTATGTT > TAAGAGATCCTATGTT.bam` Hope…
Answer: How to split a scRNA reads BAM or FASTQ file to a separate file for each cell by
by
biofalconch
▴ 580
Here is a code that should work, but just like everyone else in the comments I'm a little confused why would you need to separate them: …
Comment: Make a BedGraph file
by
kirillkirilenko
▴ 10
It works, thank you!
Comment: CNNScoreVariants Error
by
Pierre Lindenbaum
154k
check you have a complete environment for GATK , including the python module "keras". https://gatk.broadinstitute.org/hc/en-us/articles/360…
Comment: How to split a scRNA reads BAM or FASTQ file to a separate file for each cell by
by
Cathal
• 0
Did you have any luck in splitting the BAM file based on the 10x cell barcode? I would like to split a BAM file based to only include 5 spe…
Answer: Getting same value for start and end position, "DNA methylation"
by
ATpoint
72k
genomation is based on GenomicRanges which uses 1-based coordinates. https://www.biostars.org/p/84686/ Since a single CpG has a length o…
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