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1,000 results • Page
3 of 20
Sort: Votes
Rank
Views
Votes
Replies
4
votes
6
replies
622
views
Unexpected separation of RNA-seq samples on PCA plot
depletion
PCA
rRNA
plot
RNA-seq
5 months ago by
Tihana
▴ 10
4
votes
3
replies
295
views
Should you remove PCR duplicates for kmer counting?
kmer
dedup
duplicates
updated 10 weeks ago by
Darked89
4.6k • written 10 weeks ago by
ebaldwin
▴ 30
4
votes
3
replies
578
views
Over Representation analysis altered pathways in common between comparisons plot
R
Visualization
DGE
ORA
updated 6 months ago by
Basti
★ 2.0k • written 6 months ago by
Manuel
▴ 10
4
votes
12
replies
3.5k
views
How to read VCF (v4.1) file? (student project) (samtools version 0.1.19)
variant-calling
samtools
VCF
BCF
updated 25 days ago by
Ram
43k • written 5.5 years ago by
c.clarido
▴ 110
4
votes
6
replies
323
views
Protein loops
protein
Loop
5 weeks ago by
Curious
▴ 10
4
votes
7
replies
2.6k
views
low bootstrap value?
phylogeny
genome
alignment
updated 10 months ago by
Ram
43k • written 4.8 years ago by
Kumar
▴ 120
4
votes
3
replies
1.0k
views
What is the difference between vst and rlog to perform PCA ?
rlog
PCA
vsd
updated 11 months ago by
ATpoint
81k • written 11 months ago by
Amr
▴ 160
4
votes
4
replies
837
views
retaining only the clusters of interest
seurat
single-cell
scRna-seq
updated 10 months ago by
Ram
43k • written 10 months ago by
shamza
• 0
4
votes
5
replies
1.0k
views
VEP run with --af_gnomadg refuses to provide allele frequencies for extremely rare variants
vep
gnomad
updated 8 months ago by
Louisse_Ensembl
▴ 60 • written 8 months ago by
Jeremy Leipzig
22k
4
votes
6
replies
2.4k
views
Why weblogo of biopython doesn't work?
Biopython
Weblogo
updated 10 months ago by
minakshiboruahassam
• 0 • written 20 months ago by
Plus
▴ 20
4
votes
9
replies
1.1k
views
Snakemake issue with wrappers
Python
Snakemake
5 months ago by
Begonia_pavonina
▴ 150
4
votes
7
replies
2.3k
views
Batch effects vs biological variables
Batch-effect
DESeq2
combat_seq
updated 12 days ago by
Ram
43k • written 3.7 years ago by
l.uva
▴ 20
4
votes
7
replies
1.4k
views
.bed files from sequencing platform not containing intervals of "alt", "random" haplotypes. How do I perform coverage and haplotype caller?
exome
.bed
haplotypes
HG38
coverage
updated 9 months ago by
GenoMax
141k • written 9 months ago by
LeandroF.
• 0
4
votes
2
replies
547
views
Can I still remove ambient RNA if I do not have raw barcode-gene matrix?
SoupX
5 months ago by
malonzm1
▴ 20
4
votes
7
replies
760
views
Alternative for grep in a for loop
linux
updated 6 months ago by
Ram
43k • written 6 months ago by
Prangan
▴ 20
4
votes
14
replies
1.1k
views
remove white space in fastq file
fastq
updated 4 months ago by
GenoMax
141k • written 4 months ago by
gkarere
• 0
4
votes
6
replies
866
views
Hisat2 index and alignment question
ubuntu
rna-seq
index
hisat2
updated 6 months ago by
Istvan Albert
100k • written 6 months ago by
Athena
• 0
4
votes
1
reply
554
views
How to Load a Molecular Signature Database into clusterProfiler gseGO?
ClusterProfiler
RNA-seq
GSEA
updated 9 months ago by
Nitin Narwade
★ 1.6k • written 9 months ago by
Manuel Sokolov Ravasqueira
▴ 100
4
votes
7
replies
527
views
DESeq2 Multifactor Design
RNA-seq
DESeq2
updated 6 days ago by
Ram
43k • written 7 days ago by
AHerik
▴ 20
4
votes
2
replies
604
views
Visualization package for Maf Files using Python
Python
maftools
Visualization
MAF
updated 6 months ago by
Mark
★ 1.5k • written 6 months ago by
Manuel Sokolov Ravasqueira
▴ 100
4
votes
8
replies
3.5k
views
How to reduce the number of SNPs for the Lositan software
Lositan
SNP
updated 9 months ago by
Ram
43k • written 9.5 years ago by
zhaojianli198322
• 0
4
votes
3
replies
673
views
How to interpret output of PLINK association test (--assoc)
assoc
updated 8 months ago by
zx8754
11k • written 8 months ago by
karthivalarmathi99
▴ 10
4
votes
11
replies
609
views
Remove X in row name with only number
GSVA
updated 10 weeks ago by
Ram
43k • written 10 weeks ago by
Chris
▴ 260
4
votes
3
replies
473
views
Parsing columns with awk
awk
updated 5 months ago by
Ram
43k • written 5 months ago by
pablo
▴ 300
4
votes
9
replies
556
views
variant calling
variant-calling
updated 17 days ago by
Ram
43k • written 18 days ago by
dalibenam64
• 0
4
votes
13
replies
994
views
Mapping FASTQ files of scRNA-seq to reference genome
star
EBI
cellranger
scRNA-seq
SRA
updated 3 months ago by
Ram
43k • written 3 months ago by
Researcher
▴ 20
4
votes
7
replies
801
views
SNP IDs
SNP
5 months ago by
kl
▴ 10
4
votes
16
replies
930
views
hisat2 location does not exist
hisat2
updated 7 weeks ago by
Ram
43k • written 8 weeks ago by
Eric
• 0
4
votes
4
replies
630
views
Feedback on mouse brain scRNA-seq quality control
mouse
brain
singe-cell
scRNAseq
quality-control
7 months ago by
nshenoy
▴ 50
4
votes
11
replies
1.6k
views
Check Strandedness
Check_Strandedness
how_are_we_stranded_here
leafcutter
bash
updated 6 months ago by
Brian Bushnell
20k • written 8 months ago by
Y
• 0
4
votes
5
replies
773
views
Does adding reads cause batch effects?
kallisto
RNAseq
10 months ago by
bioinfo
▴ 150
4
votes
5
replies
1.1k
views
STAR mapping - regarding output files content
STAR
RNA-seq
mapping
updated 8 months ago by
rfran010
▴ 900 • written 8 months ago by
Manko47
• 0
4
votes
5
replies
1.4k
views
Distributed / parallel computing in bioinformatics
distributed-computing
updated 11 months ago by
Ram
43k • written 6.8 years ago by
CY
▴ 750
4
votes
9
replies
987
views
bcl2fastq troubleshooting all reads dumped to "Undetermined"
demultiplex
illumina
sequencing
updated 4 months ago by
GenoMax
141k • written 4 months ago by
MaxF
▴ 120
4
votes
3
replies
384
views
Single cell analysis of Cancer
cancer
single-cell
RNA-seq
updated 9 weeks ago by
GenoMax
141k • written 9 weeks ago by
moustafa_abohawya
▴ 20
4
votes
2
replies
464
views
KEGG DATABASE
DATABASE
KEGG
updated 4 months ago by
jv
★ 1.8k • written 4 months ago by
Sijjil
• 0
4
votes
3
replies
738
views
BBduk log and stats appear to be inconsistent
bbduk
bbmap
updated 11 months ago by
GenoMax
141k • written 11 months ago by
Dave Carlson
★ 1.7k
4
votes
7
replies
2.2k
views
About normalization of the datasets from Harmonized TCGA data
protein
transcript
normalisation
updated 10 weeks ago by
Ram
43k • written 21 months ago by
qiz218591
▴ 10
4
votes
8
replies
593
views
GCP Snakemake
snakemake
GCP
updated 12 weeks ago by
Ram
43k • written 12 weeks ago by
Fadwa
▴ 10
4
votes
4
replies
782
views
Segmentation fault Biopython pairwise alignment
biopython
alignment
updated 10 months ago by
Joe
21k • written 11 months ago by
antoine.fauchois92
▴ 20
4
votes
3
replies
303
views
Getting less DE genes when incorporating all samples
RNA-seq
differential-expression
deseq2
updated 9 weeks ago by
jv
★ 1.8k • written 9 weeks ago by
shome
▴ 10
4
votes
5
replies
2.4k
views
Merge CNVnator output of multiple samples
CNV
WGS
updated 9 months ago by
Ram
43k • written 6.7 years ago by
zhang248
▴ 40
4
votes
12
replies
7.7k
views
6 follow
BWA error: no ID within the read group line
bwa
readgroups
RG
parallel
updated 10 weeks ago by
mgdrnl
▴ 10 • written 3.3 years ago by
whb
▴ 60
4
votes
3
replies
575
views
Identifying enhancers that regulate certain genes
enhancers
updated 9 months ago by
rfran010
▴ 900 • written 9 months ago by
Rozita
▴ 40
4
votes
3
replies
743
views
Creating custom GTF file for use with Cellranger with barcode sequences
Cellranger
7 months ago by
stefano.iantorno
▴ 70
4
votes
6
replies
927
views
How to pass from DNA to AA fasta
genetics
updated 11 months ago by
Buffo
★ 2.4k • written 11 months ago by
Anderson Stiward
• 0
4
votes
7
replies
966
views
Statistical test to compare data across timepoints
Statistics
updated 6 months ago by
Matthias Zepper
4.5k • written 6 months ago by
Sean
▴ 20
4
votes
5
replies
530
views
Which refseq_protein db to choose for zingiberaceae
local
blastp
blast
updated 8 months ago by
GenoMax
141k • written 8 months ago by
Nilo
• 0
4
votes
13
replies
794
views
RNAseq of primary tumor and metastases in two different organ
metastases
RNA-seq
DEG
R
updated 3 days ago by
BioinfGuru
★ 1.7k • written 9 days ago by
matteo.levorato
• 0
4
votes
16
replies
1.7k
views
How to subset large BAM files specifically/ extract specific subsets?
bamtools
RNAseq
samtools
BAM
updated 8 weeks ago by
Ram
43k • written 6 months ago by
ella
• 0
1,000 results • Page
3 of 20
Recent Votes
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Answer: How can I retrieve wheat lysine non-acetylated sequences from the UniProt databa
The majority of the sequences in Trinity ID do not start from start codons. Can the sequences still be used for primer design and validation?
Answer: Cellranger count error: Input FASTQ file ended prematurely
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141k
I don't think MEGA supports GPU's: https://www.megasoftware.net/web_help_11/Part_I_Getting_Started/Installing_MEGA/System_Requirements.htm
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RG tag "L9302" is missing the the BAM header. You should have something like this in the BAM header ``` @RG ID:L9302 SM:L9302 ``` may be…
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That makes a lot more sense. Thank you.
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Type ``` help("read.idat") ``` and read the example at the bottom of the page, which shows you how to set the `other$Detection` component o…
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Accurately assessing a few QC metrics is trivially easy. Assessing the significance of variants in a clinically responsible way is really…
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If _1 and _2 really are the same library, you should rename the fastqs, or make symlinks, such that they have the same sample name, but dif…
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Just delete the index read files. They just take up space and will never be used.
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Yes. Why wouldn't you use, say, AddOrReplaceReadsGroups?
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