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1,000 results • Page
5 of 20
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Views
Votes
Replies
15
votes
34
replies
16k
views
10 follow
Issues installing bcl2fastq?
bcl2fastq
demultiplexing
updated 21 days ago by
barslmn
★ 2.1k • written 6.6 years ago by
a.rex
▴ 350
30
votes
34
replies
6.6k
views
enrichment of gene set with enrichR
enrichR
RNA-Seq
R
updated 6.0 years ago by
WouterDeCoster
47k • written 6.0 years ago by
bikash2510
▴ 30
172
votes
34
replies
26k
views
29 follow
Recommend Your Favorite Introductory "R In Bioinformatics" Books And Resources
r
books
bioconductor
updated 4 months ago by
Ram
43k • written 14.0 years ago by
Michael
54k
12
votes
34
replies
5.0k
views
Hidden Markov Models Within Sequence Analysis -- Dispelling Misconceptions + Fixing Explanations
sequencing
updated 12.0 years ago by
Fabian Bull
★ 1.3k • written 12.5 years ago by
Delinquentme
▴ 200
54
votes
34
replies
4.8k
views
13 follow
Forum:
Should We Release Database Dumps Of All Questions On Biostar?
meta
biostars
updated 13 months ago by
Ram
43k • written 13.3 years ago by
Istvan Albert
100k
36
votes
34
replies
2.7k
views
9 follow
Forum:
New to bioinformatics.....
gene
updated 10 months ago by
Ram
43k • written 6.0 years ago by
sms.00196
• 0
31
votes
34
replies
7.3k
views
11 follow
Forum:
pros- and cons- : programming skills vs. GUI
programming
lecture
updated 12 months ago by
Ram
43k • written 8.3 years ago by
TriS
★ 4.7k
80
votes
34
replies
5.2k
views
11 follow
Forum:
Authorship issues- how to resolve?
authorship
updated 14 months ago by
Ram
43k • written 8.8 years ago by
datanerd
▴ 520
15
votes
34
replies
12k
views
Improving efficiency of awk for large files
awk
updated 17 months ago by
Ram
43k • written 8.7 years ago by
AW
▴ 350
16
votes
34
replies
12k
views
6 follow
Why am I unable to load my data from a tab separated file into R?
microarray
programming
R
updated 23 months ago by
Ram
43k • written 9.1 years ago by
Mo
▴ 920
2
votes
34
replies
6.6k
views
How to install pip on HPC server
software error
6.2 years ago by
Bioinfonext
▴ 460
16
votes
34
replies
4.7k
views
7 follow
GC percent detection for several number of genes
GC%
large number of genes
7.0 years ago by
nazaninhoseinkhan
▴ 520
11
votes
34
replies
2.1k
views
De novo transcriptome from PE reads with high multi-mapping rate (Bowtie2)
RNA-Seq
read support
Assembly
bowtie2
3.5 years ago by
Dunois
★ 2.5k
19
votes
34
replies
5.5k
views
6 follow
How can I convert the blast results into a matrix?
perl
linux
python
blast
updated 2.1 years ago by
Ram
43k • written 9.3 years ago by
kandoigaurav
▴ 150
147
votes
34
replies
54k
views
17 follow
Tutorial:
Working with MAF files (Mutation Annotation Format) from the TCGA (The Cancer Genome Atlas)
music
cancer
tcga
mutation
maf
updated 13 months ago by
Ram
43k • written 11.0 years ago by
Cyriac Kandoth
6.0k
41
votes
34
replies
16k
views
10 follow
Best tool for variant calling
SNP
genome
alignment
next-gen
updated 5.4 years ago by
claire
• 0 • written 5.9 years ago by
williamsbrian5064
▴ 510
12
votes
33
replies
3.1k
views
Missing sequences in local NT database
nt
blast
ncbi
blastdbcmd
updated 5.5 years ago by
lieven.sterck
15k • written 5.5 years ago by
Prakki Rama
★ 2.7k
143
votes
33
replies
30k
views
20 follow
C/C++ Libraries For Bioinformatics?
c
c
updated 5.0 years ago by
chernouhov sergey
▴ 50 • written 13.8 years ago by
User 59
13k
70
votes
33
replies
17k
views
18 follow
Choosing Random Set Of Seqs From Larger Set
random
fasta
updated 23 months ago by
Ram
43k • written 12.0 years ago by
razor
▴ 190
6
votes
33
replies
2.7k
views
I need to understand this image
phylogenies
updated 7.1 years ago by
Emily
23k • written 7.1 years ago by
eng_samar_zayed
• 0
24
votes
33
replies
8.4k
views
Contribute To The Nat Gen Paper "Principles For The Post-Gwas Functional Characterisation Of Risk Loci"
gwas
snp
updated 13.3 years ago by
Khader Shameer
18k • written 13.3 years ago by
Giovanni M Dall'Olio
28k
27
votes
33
replies
3.7k
views
7 follow
Forum:
Biostars question catagories
statistics
biostars
meta
updated 11 months ago by
Ram
43k • written 7.4 years ago by
John
13k
296
votes
33
replies
107k
views
25 follow
Tutorial:
Cheat Sheet For One-Based Vs Zero-Based Coordinate Systems
coordinates
updated 13 months ago by
Ram
43k • written 10.4 years ago by
Obi Griffith
20k
41
votes
33
replies
18k
views
10 follow
How To Convert Xml Into A Decent Parseable Format?
xml
parsing
perl
subjective
updated 12.9 years ago by
Jrbeaman
▴ 30 • written 12.9 years ago by
Lyco
★ 2.3k
138
votes
33
replies
65k
views
19 follow
VCF files: Change Chromosome Notation
vcf
next-gen
sequence
updated 17 months ago by
Ram
43k • written 9.9 years ago by
Quak
▴ 490
10
votes
33
replies
3.7k
views
Looking for a tool like fastq screen but for ONT data
gridion
nanopore
ont
minion
updated 9 months ago by
Ram
43k • written 5.7 years ago by
Rox
★ 1.4k
27
votes
33
replies
17k
views
high % of reads mapped to multiple loci after STAR mapping
RNA-Seq
STAR
single-end
updated 6.3 years ago by
Hussain Ather
▴ 990 • written 6.3 years ago by
Lila M
★ 1.2k
48
votes
33
replies
43k
views
16 follow
Extract A Group Of Fasta Sequences From A File
fasta
python
perl
biopython
bioperl
updated 2.3 years ago by
Ram
43k • written 13.7 years ago by
Kyle
▴ 60
16
votes
33
replies
8.3k
views
9 follow
Back-filling missing genotypes in merged VCF
vcf
updated 15 months ago by
Pierre Lindenbaum
160k • written 9.4 years ago by
Katie D'Aco
★ 1.1k
11
votes
33
replies
3.9k
views
Detect Regions In A List That Are Within 1 Megabase Of Each Other
python
snp
genomics
overlap
updated 12.5 years ago by
Michael
54k • written 12.5 years ago by
Rubal
▴ 350
50
votes
33
replies
54k
views
10 follow
I would like to add gene names to a volcano plot obtained from DEseq2
RNA-Seq
DEseq2
R
updated 5.9 years ago by
Kevin Blighe
87k • written 7.7 years ago by
ta_awwad
▴ 340
29
votes
33
replies
7.8k
views
12 follow
getBM error while using bioMart
biomart
getBM
ensembl
updated 3.5 years ago by
user17394
• 0 • written 3.5 years ago by
MatStat
▴ 160
11
votes
33
replies
17k
views
How we can analyze sanger sequence chromatogram?
SNP
sequencing
alignment
sanger
updated 2.1 years ago by
Ram
43k • written 9.4 years ago by
Elnaaz
▴ 40
120
votes
33
replies
39k
views
24 follow
Forum:
Where To Look For Quality Bioinformatics Short Courses And Workshops?
Courses
updated 10 months ago by
carlopecoraro2
★ 2.4k • written 10.6 years ago by
Eric Normandeau
11k
88
votes
32
replies
9.3k
views
11 follow
Forum:
Vintage / unconventional pictures for Bioinformatics
history
picture
updated 2.0 years ago by
Ram
43k • written 9.4 years ago by
Pierre Lindenbaum
160k
129
votes
32
replies
129k
views
29 follow
Is There A Free Alternative To Ingenuity Pathway Analysis?
network
pathway
updated 24 months ago by
Ram
43k • written 13.1 years ago by
Gon
▴ 540
10
votes
32
replies
3.7k
views
6 follow
Why my CD31+ endothelial cells RNAseq didn't express CD31?
CD31
HISAT2
endothelialcells
Stringtie
RNAseq
2.9 years ago by
Youyy
• 0
153
votes
32
replies
8.4k
views
23 follow
Picking A Programming Language And Where To Begin
programming
next-gen
sequencing
c
subjective
updated 12.2 years ago by
Palani Kannan
▴ 60 • written 12.7 years ago by
Travis
★ 2.8k
82
votes
32
replies
7.6k
views
13 follow
Forum:
Shall We Go Back To Stackexchange?
meta
updated 13 months ago by
Ram
43k • written 11.3 years ago by
14134125465346445
★ 3.6k
53
votes
32
replies
13k
views
13 follow
Bio-Javascript?
updated 23 months ago by
Ram
43k • written 13.1 years ago by
Lee Katz
★ 3.1k
0
votes
32
replies
9.2k
views
DoHeatmap clusters, Seurat pipeline
scRNA-sequencing
3.5 years ago by
Morris_Chair
▴ 350
93
votes
32
replies
33k
views
26 follow
Linux Distros Best Suited For Bioinformatics?
linux
written 12.2 years ago by
Sat3Lite
▴ 150
3
votes
32
replies
3.3k
views
fastqc report for degradome reads
fastqc
adaptor
6.0 years ago by
Sam
▴ 150
32
votes
32
replies
7.9k
views
11 follow
Should We Be Using Much More Json In Our Delimited Data Formats?
gff
vcf
updated 13.2 years ago by
Erik Garrison
★ 2.4k • written 13.2 years ago by
Casbon
★ 3.3k
9
votes
32
replies
2.9k
views
Differentially gene expressed analyses of two different samples
RNA-Seq
R
next-gen
rna-seq
updated 7.3 years ago by
EVR
▴ 610 • written 7.3 years ago by
Mehmet
▴ 820
9
votes
31
replies
4.8k
views
6 follow
Clustering Million Points : Transcript Start And End Sites
clustering
updated 12.0 years ago by
Khader Shameer
18k • written 12.0 years ago by
Abhi
★ 1.6k
94
votes
31
replies
39k
views
17 follow
What Is The Quickest Algorithm For Range Overlap?
python
alignment
next-gen
sequencing
database
updated 2.0 years ago by
Ram
43k • written 13.6 years ago by
User 1586
▴ 280
10
votes
31
replies
4.3k
views
7 follow
Extract columns from a vcf file using identifiers from a second file
snp
updated 2.4 years ago by
GenoMax
140k • written 5.9 years ago by
paraskevopou
▴ 20
17
votes
31
replies
5.6k
views
Finding the best model for expression data (RNA-Seq counts)
RNA-Seq
glm
model fit
regression
updated 5.0 years ago by
i.sudbery
18k • written 5.0 years ago by
User 7754
▴ 250
24
votes
31
replies
24k
views
Calculating Allele Frequencies From Genotype Data
allele
frequency
updated 13.2 years ago by
lh3
33k • written 13.2 years ago by
Andrea_Bio
★ 2.8k
1,000 results • Page
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Comment: F*up Night style events for Bioinformatics ? Comment if you're interested!
Answer: F*up Night style events for Bioinformatics ? Comment if you're interested!
Answer: Demonstrating lack of difference between two peaksets
Comment: Input arguments for AddOrReplaceReadGroups (Picard) from fastq
Answer: Input arguments for AddOrReplaceReadGroups (Picard) from fastq
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Thanks, I modified.
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160k
11 years ago: https://www.biostars.org/p/7126/
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haha yes exactly! After the first or second ruined fasta, I started "catting" all fasta files and piping to other commands, just to reduce …
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... ha, beat me to it, posted at the same time ... this error rules them all .. here is a cool trick on how to count fasta headers in file…
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I've definitely ruined some genome fasta files by running `grep ^> mygenome.fasta` instead of `grep "^>" mygenome.fasta`
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Anyone please suggest which variant caller can be the best choice for variant calling of GBS data for polyploid plant.
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More than likely they will only be available in the accompanying analysis app (Explify RPIP) in BaseSpace. Check with Illumina tech support…
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Pretty sure I have done it, but can't remember the details. You know that thing about blocking out traumatic events ...
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Looks like those appear to be "polycomb associated non-coding RNA". You probably know what they are. https://www.ncbi.nlm.nih.gov/nuccore/…
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