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797 results • Page
1 of 16
Sort: replies
Rank
Views
Votes
Replies
298
votes
122
replies
28k
views
29 follow
Mean Length Of Fasta Sequences
code
fasta
sequence
codegolf
updated 19 days ago by
jena
▴ 270 • written 13.2 years ago by
Eric Normandeau
11k
146
votes
70
replies
46k
views
20 follow
Tutorial:
Network plot from expression data in R using igraph
microarray
RNA-Seq
R
network
updated 26 days ago by
Raheleh
▴ 260 • written 5.8 years ago by
Kevin Blighe
86k
162
votes
64
replies
80k
views
39 follow
Selecting Random Pairs From Fastq?
random
fastq
illumina
sequence
updated 4 days ago by
rohitsatyam102
▴ 750 • written 12.5 years ago by
Ketil
4.1k
170
votes
41
replies
91k
views
27 follow
Multiline Fasta To Single Line Fasta
fasta
updated 22 hours ago by
Ram
40k • written 12.3 years ago by
Palu
▴ 250
100
votes
38
replies
28k
views
34 follow
Forum:
List of cloud genomics companies
cloud-genomics
updated 24 days ago by
Jeremy Leipzig
21k • written 9.9 years ago by
14134125465346445
★ 3.6k
105
votes
26
replies
40k
views
23 follow
How To Create Mutation Diagram In R Or In Any Tools?
mutation
domain
r
updated 5 days ago by
zx8754
11k • written 10.7 years ago by
henryvuong
▴ 810
38
votes
25
replies
8.1k
views
13 follow
FASTA file of fixed length
sequence
fasta
updated 10 days ago by
Ram
40k • written 7.5 years ago by
waqasnayab
▴ 250
35
votes
23
replies
27k
views
11 follow
bcftools: error while loading shared libraries: libcrypto.so.1.0.0: cannot open shared object file: No such file or directory
bcftools
updated 21 days ago by
s.w.vanderlaan
▴ 40 • written 2.2 years ago by
Michal Nevo
▴ 110
33
votes
23
replies
18k
views
12 follow
Is there a tool that sorts gtf files?
RNA-Seq
genome
updated 10 days ago by
alejandrogzi
▴ 30 • written 5.5 years ago by
JJ
▴ 660
18
votes
22
replies
8.0k
views
10 follow
Tutorial:
Create de novo repeat library
de-novo
repeat
annotation
updated 23 hours ago by
evoecogen
▴ 20 • written 3.8 years ago by
Juke34
8.2k
60
votes
21
replies
2.8k
views
14 follow
Reproduce the article "The complete sequence of a human genome."
genome
assembly
updated 22 days ago by
Michael
53k • written 23 days ago by
sqshigg
▴ 60
81
votes
21
replies
40k
views
15 follow
How To Get Bed File Containing Exons Of Canonical Transcripts And Their Corresponding Gene Symbols
bed
transcript
ucsc
biomart
updated 9 days ago by
Joel Wallenius
▴ 180 • written 9.6 years ago by
pristanna
▴ 750
2
votes
20
replies
1.5k
views
The number of SVs called by `vg call` is much smaller than the number of SVs in the VCF used to construct the graph
vg
16 days ago by
Maxine
▴ 30
10
votes
18
replies
3.1k
views
how to identify CDR region in antibody sequence
CDR
antibody
updated 22 days ago by
Ram
40k • written 15 months ago by
reany
▴ 50
75
votes
18
replies
2.0k
views
11 follow
Blog:
A list of technical advantages of Snakemake over Nextflow | Cloud solution for Snakemake
Snakemake
updated 4 days ago by
Ram
40k • written 9 days ago by
Kenny
▴ 30
8
votes
17
replies
1.1k
views
7 follow
How to limit fasta header to 40 characters?
unix
seqkit
fasta
updated 16 days ago by
Roop
• 0 • written 18 days ago by
fishingline37
• 0
16
votes
16
replies
1.8k
views
Species identifcation using 16s rRNA
16srRNA
fasta
updated 2 days ago by
Ram
40k • written 2.6 years ago by
A_heath
▴ 140
36
votes
16
replies
28k
views
14 follow
Generating consensus sequence from bam file
genome
samtools
bwa
fasta
updated 3 days ago by
jkbonfield
★ 1.1k • written 4.6 years ago by
chparada
▴ 60
7
votes
15
replies
3.3k
views
Demultiplexing based on dual indices in headers while allowing 1 mismatch to each index
next-gen
sequencing
updated 4 days ago by
Gabriel R.
★ 2.9k • written 3.3 years ago by
Rezenman
• 0
18
votes
14
replies
26k
views
7 follow
removing batch effects using ComBat and SVA
R
ComBat
SVA
Batch effect
updated 29 days ago by
maximal_life
▴ 20 • written 7.3 years ago by
LJ
▴ 260
8
votes
14
replies
1.8k
views
How to remove fasta headers in a multifasta file and write file name as a fasta header?
gene
sequence
genome
alignment
next-gen
updated 15 days ago by
Joe
21k • written 2.9 years ago by
Kumar
▴ 120
19
votes
14
replies
793
views
Forum:
What is the amount of sequencing data produced annually?
data
research
sequencing
updated 3 days ago by
Jeremy Leipzig
21k • written 3 days ago by
vincenthus
▴ 70
124
votes
13
replies
165k
views
13 follow
How Can I Convert Bam To Sam?
bam
next-gen-sequencing
sam
updated 18 days ago by
Ram
40k • written 13.2 years ago by
Biomed
4.9k
2
votes
13
replies
579
views
Dealing with transcriptome sequences that are smaller than their respective genes
blastn
Trinity
Transcriptome
RNA-seq-analysis
De-novo-transcriptome-assembly
1 day ago by
langziv
▴ 50
13
votes
13
replies
6.5k
views
6 follow
Extract SNPs flanking sequences based on VCF and genome Fasta files
snp
sequence
genome
updated 25 days ago by
LauGuillardin
• 0 • written 5.1 years ago by
Denis
▴ 280
10
votes
13
replies
12k
views
6 follow
How to annotate only selected genes on a heatmap
R
updated 18 days ago by
GenoMax
134k • written 6.3 years ago by
h.fushimi.x689
▴ 30
7
votes
13
replies
677
views
Help with Error: Required version of NumPy not available: installation of Numpy >= 1.6 not found
seurat
leiden
22 days ago by
Chris
▴ 180
0
votes
13
replies
475
views
STAR Intron Motif Script Gives Segmentation fault Error
STAR
Linux
3 hours ago by
Y
• 0
4
votes
12
replies
811
views
bedops alternative for bedtools -unionbedg ?
bedtools
bam
coverage
bedops
bed
updated 7 days ago by
Alex Reynolds
35k • written 24 days ago by
Agastya
▴ 10
4
votes
12
replies
3.4k
views
6 follow
Sort gff3 on chromosome, position and then featuretype (gene, mRNA, exon, CDS)
gff3
updated 10 days ago by
alejandrogzi
▴ 30 • written 3.4 years ago by
William
★ 5.2k
9
votes
12
replies
4.2k
views
converting a list of genes and interaction to a graph
gene
R
updated 3 days ago by
Amirhossein Hajianpour
▴ 40 • written 7.7 years ago by
fi1d18
★ 4.2k
5
votes
12
replies
771
views
6 follow
Formatting RNA-Seq Data for Kruskal Wallis Test on R
R
Kruskal-Wallis
RNA-seq
updated 28 days ago by
swbarnes2
13k • written 4 weeks ago by
eco2249
• 0
23
votes
12
replies
1.9k
views
Genes encoded on both strands of DNA?
Genes
strand
updated 2 days ago by
Ram
40k • written 16 months ago by
A_heath
▴ 140
1
vote
12
replies
2.2k
views
Confused about % of mapped and unmapped reads output from STAR aligner
RNAseq
STAR
updated 9 days ago by
Ram
40k • written 11 months ago by
mohsamir2016
▴ 30
5
votes
12
replies
791
views
Converting custom VCF to standard VCF
VCF
9 days ago by
avelarbio46
▴ 30
2
votes
11
replies
1.4k
views
RepeatMasker error when trying to generate repeat sequence distribution pie chart (all code and errors provided)
repeatmasker
updated 23 days ago by
rfran010
▴ 790 • written 5 weeks ago by
epianalysis
• 0
10
votes
11
replies
1.2k
views
Seeking feedback on ChIP-seq normalization method: Calculating scaling factors by dividing input by IP, including spike-in
coverage
spike-in
scaling-factor
ChIP-seq
14 days ago by
kalavattam
▴ 180
0
votes
11
replies
691
views
Normalization for microarrays >1000+ samples?
microarray
normalization
oligo
3 days ago by
evmae
• 0
2
votes
11
replies
801
views
Extracting regions around sites in VCF file and writing them as fasta sequences/files
VCF
fasta
updated 11 days ago by
GenoMax
134k • written 24 days ago by
Aiswarya
▴ 10
2
votes
11
replies
552
views
Qualimap bamqc with very high N%
qualimap
28 days ago by
Priyanka
▴ 10
3
votes
10
replies
434
views
STAR index not working
STAR
RNA-Seq
1 day ago by
camillab.
▴ 130
1
vote
10
replies
876
views
Deepvariant variant calling by singularity
deepvariant
singularity
conda
docker
updated 12 hours ago by
jeffhsu3
• 0 • written 11 weeks ago by
fra.silvestro99
▴ 10
6
votes
10
replies
695
views
Making pairwise matrix using ChIP-Seq peak binding matrix in R
R
matrix
binding
Chip-seq
18 days ago by
Ankit
▴ 390
19
votes
10
replies
29k
views
6 follow
read depth using samtools
depth
samtools
updated 9 days ago by
Sachin
• 0 • written 4.7 years ago by
LimMo
▴ 30
3
votes
10
replies
2.2k
views
Salmon alignment based quantification
Salmon
rna-seq
quantification
updated 1 day ago by
Mat
▴ 60 • written 18 months ago by
edus_bioinfo
▴ 40
19
votes
10
replies
825
views
Forum:
Pain points using commercial clouds
gpt
tinybio
updated 8 days ago by
vincenthus
▴ 70 • written 23 days ago by
Sasha
▴ 720
7
votes
10
replies
469
views
Batch effect normalization
RNA-seq
batch-effect
updated 5 days ago by
Ram
40k • written 5 days ago by
Smriti
• 0
6
votes
10
replies
731
views
Create a reference genome from aligned bam file
bam
bam2fasta
fasta
29 days ago by
Vincent
▴ 20
8
votes
10
replies
673
views
Inflated GWAS test statistic after merging multiple batches of genotype dataset imputed differently
genotype
imputation
gwas
updated 2 days ago by
LauferVA
3.7k • written 4 days ago by
Amy
▴ 20
2
votes
10
replies
4.4k
views
CWL: Getting the outputs(File) of a command line tool
Common-Workflow-Language
cwl
updated 11 days ago by
Ram
40k • written 6.4 years ago by
kevin.o.oluoch
▴ 70
797 results • Page
1 of 16
Recent Votes
Answer: Ties in reranked list
Answer: Ties in reranked list
Comment: Error: cannot open file 2 for reading From Cufflinks Version 2.2.1 When Attempti
Comment: Error in bowtie2
Recommended Tools For Alternative Splicing Detection From Rna-Seq Data
Comment: Using STAR aligner to build index of hg38
Answer: How to sort using samtools
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Recent Replies
Comment: Ties in reranked list
by
Hamza
• 0
I had actually accidentally used ranks instead of Entrez gene ids (but switched later to human Ensembl gene ids). However, without your com…
Comment: Hugo_Symbol to Entrez ID
by
shakyaram079
• 0
Yes sure. These are all gene IDs BZRAP1, C19orf60, TCEB3 and so on.
Comment: Error: cannot open file 2 for reading From Cufflinks Version 2.2.1 When Attempti
by
Y
• 0
I tried the commands you recommended in the bash/command line. When I tried `find "${bam_directory}" -type f -name "*.bam" | xargs samtools…
Comment: Hugo_Symbol to Entrez ID
by
GenoMax
134k
Can you provide some examples of HUGO ID's you are unable to convert?
Comment: Using STAR aligner to build index of hg38
by
GenoMax
134k
GTF file includes gene models/annotation information. You could also use a program like `salmon/kallisto` with just human transcriptome to…
Comment: Error: cannot open file 2 for reading From Cufflinks Version 2.2.1 When Attempti
by
Pierre Lindenbaum
157k
then test each files. find "${bam_directory}" -type f -name "*.bam" | xargs samtools quickcheck file "${reference_gen…
Answer: Ties in reranked list
by
alserg
▴ 860
The problem here is not the ties, but that your gene IDs in the pathway list (ensemble human genes) does not match the names of the stats v…
Comment: Error: cannot open file 2 for reading From Cufflinks Version 2.2.1 When Attempti
by
Y
• 0
I did not use the space between the `-u` flag and the `-o` flag (the blank line) but I did do what you recommended: # Run CuffDiff wit…
Answer: Error: cannot open file 2 for reading From Cufflinks Version 2.2.1 When Attempti
by
Pierre Lindenbaum
157k
how about simply trying: ``` cuffdiff -u "${annotation_gtf}" \ -o "${output_directory}" \ -b "${reference_genome}" \ -p "${num_th…
Comment: Using STAR aligner to build index of hg38
by
Grace
• 0
Yes, I know also need a GTF file. So the GTF file will include RNA information? Thanks for your answer!!
Comment: STAR Intron Motif Script Gives Segmentation fault Error
by
Y
• 0
I will try and figure it out on my own given what you all have mentioned. Thank you for your time.
Comment: Using STAR aligner to build index of hg38
by
Amitm
★ 2.2k
Have you gone through the manual [here][1]. In addition to the genome fasta file, you would also need a GTF file (of gene annotations) to b…
Comment: Highly inflated p-values in GWAS by regenie
by
4galaxy77
2.8k
You still definitely need to include principle components as covariates, even if your data is from the same ethnicity. Not including those …
Answer: How to create structural variants ground truth for alignment of two long-read ge
by
Christophe
• 0
Hi, D-genies is using minimap2 to align both genomes and minimap2 is chaining local alignments to produce a global one. If the SV are sm…
Comment: Ties in reranked list
by
Hamza
• 0
In this case there are no results in my fgsea object unfortunately
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