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863 results • Page
2 of 18
Sort: Votes
Rank
Views
Votes
Replies
25
votes
8
replies
11k
views
6 follow
Tools For Chipseq Scale Motif Finding?
motif
motif
chip-seq
updated 23 days ago by
Ram
41k • written 13.7 years ago by
Cassj
★ 1.3k
25
votes
10
replies
13k
views
10 follow
Retrieve GFF3 file from ncbi
gff3
ncbi
efetch
updated 28 days ago by
Cornelius
▴ 70 • written 5.8 years ago by
john
▴ 110
24
votes
9
replies
10k
views
6 follow
Exploring Snp Data
snp
association
updated 17 days ago by
Ram
41k • written 13.6 years ago by
Bioch'Ti
★ 1.1k
24
votes
14
replies
8.1k
views
9 follow
How To Find All Gwas Studies That A Given Gene Has Been Implicated In?
gwas
gene
genome
updated 23 days ago by
Ram
41k • written 13.7 years ago by
Andrew Su
4.9k
24
votes
11
replies
10k
views
How To Download All Est Sequences For Organism Xx From Ncbi?
eutils
genbank
updated 23 days ago by
Ram
41k • written 13.7 years ago by
Yannick Wurm
★ 2.5k
24
votes
12
replies
7.1k
views
8 follow
Randomize Read Order In Multigbp Fastq File?
fastq
updated 24 days ago by
Brian Bushnell
19k • written 12.4 years ago by
2184687-1231-83-
★ 5.1k
23
votes
4
replies
34k
views
bcftools compressing and indexing vcf files
sequence
bcftools
vcf
index
updated 25 days ago by
GenoMax
136k • written 5.2 years ago by
Inquisitive8995
▴ 270
23
votes
9
replies
6.8k
views
What 3Rd Generation Sequencing Methods Are Out There
next-gen-sequencing
updated 20 days ago by
Ram
41k • written 13.7 years ago by
Istvan Albert
99k
23
votes
21
replies
7.7k
views
9 follow
fastest UMAP method
UMAP
R
updated 16 days ago by
Mensur Dlakic
★ 25k • written 4.1 years ago by
grey
▴ 30
22
votes
8
replies
8.5k
views
7 follow
Gene Expression: Clustering Co-Expressed Genes
gene
clustering
microarray
updated 20 days ago by
Ram
41k • written 13.7 years ago by
Eric Normandeau
11k
22
votes
21
replies
4.4k
views
7 follow
Quick Programming Challenge: Calculate Common And Unique Regions From A List Of Chromosome Segments
programming
updated 17 days ago by
Ram
41k • written 13.6 years ago by
Khader Shameer
18k
22
votes
7
replies
24k
views
What Does The "N50" Mean?
assembly
updated 17 days ago by
Ram
41k • written 13.6 years ago by
Bioch'Ti
★ 1.1k
21
votes
13
replies
9.9k
views
8 follow
Blast Motif With Regular Expression ?
blast
motif
updated 17 days ago by
Ram
41k • written 13.6 years ago by
Markus Krupp
▴ 80
21
votes
11
replies
2.0k
views
6 follow
Forum:
Rust bioinformatics projects ideas
projects
scRNA-seq
RNA-seq
Rust
updated 9 days ago by
Jeremy Leipzig
22k • written 9 months ago by
bompipi95
▴ 140
20
votes
5
replies
3.2k
views
How Do I Import Data From A Torrent Into A Bioperl, R, Bioclipse, Or Taverna Application?
R
bioperl
torrent
updated 23 days ago by
Ram
41k • written 13.7 years ago by
Egon Willighagen
5.4k
20
votes
14
replies
4.7k
views
6 follow
Hardware Resources For Hpc In Bioinformatics
hpc
updated 23 days ago by
Ram
41k • written 13.7 years ago by
Jarretinha
3.4k
20
votes
10
replies
14k
views
8 follow
Test Whether The Variance In A Group Is Lower Than In Another
statistics
r
updated 23 days ago by
Ram
41k • written 13.7 years ago by
Giovanni M Dall'Olio
28k
19
votes
13
replies
7.9k
views
10 follow
Tutorial:
Setting up Aspera Connect (ascp) on Linux and macOS
ascp
aspera
updated 29 days ago by
jude
• 0 • written 17 months ago by
ATpoint
78k
18
votes
20
replies
3.9k
views
9 follow
Is There Any Useful Information To Be Gathered Analyzing The Genomes Of Different Populations Of Cicadas?
project
education
updated 23 days ago by
Ram
41k • written 13.7 years ago by
Scott
▴ 70
17
votes
3
replies
2.6k
views
Forum:
How to Use Biostars Part-3: Formatting Text and Using GitHub Gists
meta
how-to
documentation
10 days ago by
Ram
41k
17
votes
11
replies
3.6k
views
Which Is The Most Accurate Method To Align Multiple Nucleotide Sequences Without Prior Information?
alignment
sequence
updated 17 days ago by
Ram
41k • written 13.6 years ago by
Michael Barton
★ 1.8k
17
votes
14
replies
13k
views
10 follow
Converting Ab1 Trace Files Into Scf Trace Files
sequence
updated 20 days ago by
Ram
41k • written 13.7 years ago by
Will
4.5k
17
votes
2
replies
3.8k
views
Which Google Summer Of Code Projects Are Available For Bioinformatics In 2010?
project
updated 23 days ago by
Ram
41k • written 13.7 years ago by
Giovanni M Dall'Olio
28k
17
votes
4
replies
5.9k
views
Artemis, Apollo Or Anything For Genome Annotation Editing With Next Gen Sequence Data
genome
next-gen-sequencing
annotation
updated 17 days ago by
Ram
41k • written 13.6 years ago by
Darked89
4.5k
17
votes
7
replies
3.9k
views
How Difficult/Reliable Is It To Programmatically (Python) Look Up And Download Papers?
literature
python
text
updated 23 days ago by
Ram
41k • written 13.7 years ago by
Rvidal
▴ 270
16
votes
3
replies
4.3k
views
A Grep For Gene Ontology ?
gene
GO
updated 20 days ago by
Ram
41k • written 13.6 years ago by
Pierre Lindenbaum
158k
16
votes
4
replies
10k
views
Do P-Values From A Generalised Linear Model Need Correction For Multiple Testing?
statistics
r
multiple
updated 20 days ago by
Ram
41k • written 13.7 years ago by
Phis
★ 1.1k
16
votes
11
replies
8.2k
views
7 follow
Where To Find The Genome Sizes Of Sequenced Plant Species?
plant-genome
updated 23 days ago by
Ram
41k • written 13.7 years ago by
Zhaorong
★ 1.4k
16
votes
13
replies
5.3k
views
Som For Detection Matlab
disease
matlab
updated 17 days ago by
Ram
41k • written 13.6 years ago by
Tim
▴ 110
15
votes
20
replies
1.1k
views
Bbtools callvariant multisample mode, + base recalibration
Bbtools
7 days ago by
Axzd
▴ 50
15
votes
16
replies
4.6k
views
Gene Expression Experiment Using Ngs Data
next-gen-sequencing
gene-expression
updated 17 days ago by
Ram
41k • written 13.6 years ago by
Eric Normandeau
11k
15
votes
22
replies
8.3k
views
What Are The Most Reliable Normalization Methods For Microarrays?
microarray
updated 23 days ago by
Ram
41k • written 13.7 years ago by
Jarretinha
3.4k
14
votes
5
replies
4.4k
views
How To Search Disease-Causing Chromosomal Structure Variation?
cnv
structural-variant
sv
updated 23 days ago by
Ram
41k • written 13.7 years ago by
Ma_Ko
▴ 100
14
votes
6
replies
6.0k
views
What Tool Should I Use To Assemble Data Produced By A 454 Sequencer?
assembly
next-gen-sequencing
updated 17 days ago by
Ram
41k • written 13.6 years ago by
Cupton
▴ 80
14
votes
10
replies
3.4k
views
6 follow
Should I remove Kmers identified in FastQC?
Illumina
fastqc
NGS
updated 11 days ago by
GenoMax
136k • written 7.7 years ago by
Randomguy
▴ 30
14
votes
1
reply
10k
views
From A Geo Gsm Id, How To Obtain The Corresponding Raw File(S) Hosted On Sra?
fastq
r
bioconductor
sra
geo
updated 17 days ago by
Ram
41k • written 13.6 years ago by
Nico
▴ 190
13
votes
3
replies
3.3k
views
Amino Acid Content Statistical Test
statistics
amino-acids
updated 23 days ago by
Ram
41k • written 13.7 years ago by
Noyk
▴ 100
13
votes
11
replies
3.8k
views
Tagging Pubmed With Umls
pubmed
text
updated 17 days ago by
Ram
41k • written 13.6 years ago by
Christiank
▴ 70
13
votes
5
replies
6.8k
views
How To Align Reads Obtained From Sequence Capture
exome-sequencing
next-gen-sequencing
sequence
updated 17 days ago by
Ram
41k • written 13.6 years ago by
Istvan Albert
99k
13
votes
6
replies
9.0k
views
What To Do With An Error In The Fastq Illumina Quality Scores
fastx-toolkit
next-gen-sequencing
fastq
updated 17 days ago by
Ram
41k • written 13.6 years ago by
Allpowerde
★ 1.3k
13
votes
11
replies
15k
views
10 follow
TCGA/Broad Institute CNV Files Segment Mean
tcga
cnv
updated 6 days ago by
sativus
▴ 10 • written 9.2 years ago by
dirigible2012
▴ 320
13
votes
7
replies
6.0k
views
Go Functional Annotation
gene
software
updated 20 days ago by
Ram
41k • written 13.6 years ago by
Noyk
▴ 100
13
votes
6
replies
350
views
6 follow
how to sort fasta file according to a header file
fasta
updated 9 days ago by
Ram
41k • written 9 days ago by
Nelo
▴ 20
12
votes
4
replies
4.5k
views
How To Retrive The Dna Sequence From A List Of Embl And Geneid
genbank
dna
protein
uniprot
updated 23 days ago by
Ram
41k • written 13.7 years ago by
Kirsley
▴ 50
12
votes
4
replies
9.4k
views
How To Compute Dn/Ds Ratio And Get Descriptive Statistics On Thousands Of Sequences ?
selection
statistics
next-gen
snp
updated 17 days ago by
Ram
41k • written 13.6 years ago by
Bioch'Ti
★ 1.1k
12
votes
11
replies
7.9k
views
8 follow
Parsing Ace File To Fasta Formated Alignement
fasta
updated 20 days ago by
Ram
41k • written 13.7 years ago by
Eric Normandeau
11k
12
votes
3
replies
6.0k
views
How To Mask Low-Complexity Regions In Proteins?
protein
software
updated 17 days ago by
Ram
41k • written 13.6 years ago by
Michael Kuhn
5.0k
12
votes
15
replies
4.3k
views
8 follow
for go enrichment analysis which tool do you recommend?
RNA-Seq
go
updated 28 days ago by
Hamid Ghaedi
3.1k • written 3.2 years ago by
eridanus
▴ 40
11
votes
6
replies
684
views
6 follow
UMAP or TSNE for single cells?
single-cell
updated 7 days ago by
jamesxli2007
▴ 40 • written 14 days ago by
synat.keam
▴ 80
11
votes
4
replies
4.9k
views
Searching For Microsatellites Motifs In Ngs Data
next-gen
sequencing
updated 20 days ago by
Ram
41k • written 13.6 years ago by
Bioch'Ti
★ 1.1k
863 results • Page
2 of 18
Recent Votes
Answer: 1000 genomes project reference panel - GRCh38
Answer: 1000 genomes project reference panel - GRCh38
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If you have an organism that lacks the GO to gene mapping then you have to find a way to assign these terms to your genes. Basically your …
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you have not mentioned what kind of resources you have, how much data you have to process and what the expected genome/transcriptome sizes …
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Its not my data. An external researcher is visiting and she wanted from us to do some bioinformatics... The samples were not sequenced by u…
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Oh, I understand. Thank you so much for your help! The truth is that there is so much information, so many packages, libraries, tutorials,…
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They could have saved themselves a ton of money by sequencing this on a miseq.
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I think there are tools like ragtag https://github.com/malonge/RagTag that could help. you can also align your reads back to your new assem…
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Hi, did you find an effective solution for this problem? beside Agat and
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alice005201314
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Thank you. I asked a stupid question.
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First hit on google: https://stackoverflow.com/questions/73935357/error-in-grid-callc-convert-x-as-integerwhatfrom-as-integerwhatto-vie
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Hi, Scaling all features might be useful to plot genes that are not among the 2k HVG in a heatmap. Otherwise than that, I never encounter…
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