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comments
0
votes
1
reply
616
views
Do we have any disease specific SNVs database?
cancer
mutation
SNP
SNV
database
updated 18 months ago by
Medhat
9.8k • written 18 months ago by
Nemo
• 0
1
vote
2
replies
630
views
How should I interpret FB_Plot in microarray analysis?
microarray
analysis
control
quality
updated 18 months ago by
Ram
44k • written 18 months ago by
Nemo
• 0
0
votes
6
replies
1.1k
views
zero byte files in sratoolkit.3.0.1-ubuntu64
fastq
sra-toolkit
rna-seq
updated 19 months ago by
Ngrin
• 0 • written 19 months ago by
Nemo
• 0
7
votes
4
replies
1.1k
views
Processed RNA seq data publicly available
RNA-seq
updated 18 months ago by
Ram
44k • written 20 months ago by
Nemo
• 0
0
votes
3
replies
864
views
Combining multiple datasets increases the fgsea p-value
enrichment
fgsea
dataset
updated 20 months ago by
mark.ziemann
★ 1.9k • written 20 months ago by
Nemo
• 0
0
votes
0
replies
864
views
Comment:
Comment: Combining multiple datasets increases the fgsea p-value
20 months ago by
Nemo
• 0
0
votes
1
reply
717
views
Comment:
Comment: What is the default/best practice to map prob IDs to gene IDs
21 months ago by
Nemo
• 0
2
votes
3
replies
717
views
What is the default/best practice to map prob IDs to gene IDs
gsea
map
gene
prob
updated 21 months ago by
barslmn
★ 2.3k • written 21 months ago by
Nemo
• 0
2
votes
2
replies
693
views
Question regarding pathways and cell types
signaling
types
cell
pathway
updated 21 months ago by
LauferVA
4.4k • written 21 months ago by
Nemo
• 0
0
votes
0
replies
745
views
Comment:
Comment: predict gain/ loss of function from mutation
22 months ago by
Nemo
• 0
0
votes
1
reply
745
views
Comment:
Comment: predict gain/ loss of function from mutation
22 months ago by
Nemo
• 0
0
votes
3
replies
745
views
predict gain/ loss of function from mutation
protein
mutation
loss
gain
22 months ago by
Nemo
• 0
2
votes
1
reply
602
views
Get variant type from genotype data
type
missense
mutation
nonsense
variant
updated 22 months ago by
Sam
★ 4.8k • written 22 months ago by
Nemo
• 0
0
votes
1
reply
859
views
Comment:
Comment: Htseq-count output file having a high number of __not_aligned
23 months ago by
Nemo
• 0
0
votes
3
replies
859
views
Htseq-count output file having a high number of __not_aligned
read
htseq-count
human
counts
genome
alignment
updated 23 months ago by
Shred
★ 1.5k • written 23 months ago by
Nemo
• 0
0
votes
0
replies
317
views
The region for RNase P gene in human genome
gene
genome
read
count
23 months ago by
Nemo
• 0
0
votes
1
reply
510
views
How parse collectReadCounts output in r?
CollectReadCounts
r
gatk
rstudio
updated 23 months ago by
Istvan Albert
101k • written 23 months ago by
Nemo
• 0
0
votes
0
replies
865
views
Comment:
Comment: Get distribution of enrichment scores across all permutations in fgsea
23 months ago by
Nemo
• 0
3
votes
1
reply
542
views
aligning RNA seq data against human genome
variant
calling
rna-seq
alignment
updated 23 months ago by
GenoMax
145k • written 23 months ago by
Nemo
• 0
0
votes
1
reply
865
views
Comment:
Comment: Get distribution of enrichment scores across all permutations in fgsea
23 months ago by
Nemo
• 0
0
votes
3
replies
865
views
Get distribution of enrichment scores across all permutations in fgsea
enrichment
gsea
pathway
analysis
fgsea
permutation
23 months ago by
Nemo
• 0
0
votes
1
reply
618
views
Normalizing read counts while having multiple group of samples with different conditions
FPKM
normalizing
rna-seq
read-count
alignment
updated 24 months ago by
seidel
11k • written 24 months ago by
Nemo
• 0
0
votes
0
replies
533
views
Comment:
Comment: Normalized read counts with FPKM
2.0 years ago by
Nemo
• 0
0
votes
1
reply
533
views
Normalized read counts with FPKM
Read
FPKM
Normalize
count
RNA-Sequnce
2.0 years ago by
Nemo
• 0
0
votes
1
reply
651
views
Comment:
Comment: How can I get the number of reads per variant in hisat2?
2.0 years ago by
Nemo
• 0
1
vote
3
replies
651
views
How can I get the number of reads per variant in hisat2?
alignemnt
variant
gatk
covid
hisat2
updated 2.0 years ago by
Arup Ghosh
3.2k • written 2.0 years ago by
Nemo
• 0
0
votes
1
reply
798
views
Comment:
Comment: What is chrom and position values in Wuhan-Hu-1 genome data
2.0 years ago by
Nemo
• 0
2
votes
3
replies
798
views
What is chrom and position values in Wuhan-Hu-1 genome data
alignemnt
variant
gatk
covid
hisat2
updated 2.0 years ago by
GenoMax
145k • written 2.0 years ago by
Nemo
• 0
0
votes
0
replies
990
views
Comment:
Comment: Why there are variants of covid (delta and omicron) in normal samples?
2.0 years ago by
Nemo
• 0
0
votes
1
reply
990
views
Comment:
Comment: Why there are variants of covid (delta and omicron) in normal samples?
2.0 years ago by
Nemo
• 0
0
votes
1
reply
990
views
Comment:
Comment: Why there are variants of covid (delta and omicron) in normal samples?
2.0 years ago by
Nemo
• 0
1
vote
6
replies
990
views
Why there are variants of covid (delta and omicron) in normal samples?
alignemnt
variant
gatk
covid
hisat2
2.0 years ago by
Nemo
• 0
0
votes
1
reply
1.3k
views
Comment:
Comment: What is --known-sites in BaseRecalibration of GATK
2.0 years ago by
Nemo
• 0
0
votes
1
reply
1.3k
views
Comment:
Comment: What is --known-sites in BaseRecalibration of GATK
2.0 years ago by
Nemo
• 0
0
votes
5
replies
1.3k
views
What is --known-sites in BaseRecalibration of GATK
rna-seq
gatk
variants
site
baserecalibration
updated 2.0 years ago by
Arup Ghosh
3.2k • written 2.0 years ago by
Nemo
• 0
2
votes
1
reply
795
views
Can MarkDuplicates of Picard be used for RNA reads?
variants
MarkDuplicates
rna
picard
updated 2.0 years ago by
LChart
4.2k • written 2.0 years ago by
Nemo
• 0
1
vote
1
reply
782
views
Problem in MarkDuplicates of picard
variants
MarkDuplicates
picard
rna
updated 2.0 years ago by
Pierre Lindenbaum
163k • written 2.0 years ago by
Nemo
• 0
0
votes
1
reply
1.2k
views
Comment:
Comment: using gatk haplotypecaller for variants extraction
2.0 years ago by
Nemo
• 0
0
votes
3
replies
1.2k
views
using gatk haplotypecaller for variants extraction
variants
gatk
haplotypecaller
rna-seq
updated 2.0 years ago by
Ram
44k • written 2.0 years ago by
Nemo
• 0
0
votes
0
replies
764
views
Comment:
Comment: Splice aware or not for RNA sequence data
2.0 years ago by
Nemo
• 0
1
vote
2
replies
764
views
Splice aware or not for RNA sequence data
splice
RNA
hisat2
sequence
alignment
2.0 years ago by
Nemo
• 0
0
votes
0
replies
402
views
CalibrateDragstrModel - Not enough cases to estimate parameters, using defaults
dragen-os
calibration
gatk
dragen
alignment
2.0 years ago by
Nemo
• 0
0
votes
0
replies
431
views
Control detected variants for normal samples in dragen
calling
illumina
variants
dragen
alignment
2.1 years ago by
Nemo
• 0
0
votes
9
replies
2.1k
views
Not producing sam file in hisat2
sam
hisat2
header
alignment
updated 23 months ago by
Ambu Vijayan
▴ 30 • written 2.1 years ago by
Nemo
• 0
0
votes
0
replies
2.1k
views
Answer:
Answer: Not producing sam file in hisat2
2.1 years ago by
Nemo
• 0
0
votes
1
reply
2.1k
views
Comment:
Comment: Not producing sam file in hisat2
2.1 years ago by
Nemo
• 0
0
votes
0
replies
2.1k
views
Comment:
Comment: Not producing sam file in hisat2
2.1 years ago by
Nemo
• 0
0
votes
0
replies
1.8k
views
Comment:
Comment: Adding @RG header line to bam and sam files in hisat2
2.1 years ago by
Nemo
• 0
0
votes
1
reply
2.1k
views
Comment:
Comment: Not producing sam file in hisat2
2.1 years ago by
Nemo
• 0
0
votes
1
reply
1.8k
views
Comment:
Comment: Adding @RG header line to bam and sam files in hisat2
2.1 years ago by
Nemo
• 0
64 results • Page
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