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122,007 results • Page
271 of 2441
Sort: Rank
Rank
Views
Votes
Replies
0
votes
1
reply
878
views
Adding your own script to a Singularity image.
singularity
updated 2.5 years ago by
ATpoint
89k • written 2.5 years ago by
Anjan
▴ 850
4
votes
4
replies
1.4k
views
16S FASTQC report and removing over represented and duplicate sequences.
trimming
fastqc
2.5 years ago by
JNV
▴ 10
1
vote
1
reply
874
views
GSNAP insufficient memory error
mapping
GSNAP
2.5 years ago by
Hood
▴ 40
1
vote
3
replies
1.2k
views
samtools and bowtie2 alignment
alignment
samtools
bowtie2
updated 2.5 years ago by
GenoMax
154k • written 2.5 years ago by
qudrat.nii
▴ 40
1
vote
4
replies
1.4k
views
Clarification on conceptual question regarding ORF-calling
ORFIPY
ORF
2.5 years ago by
Daniel
▴ 40
0
votes
1
reply
824
views
Is there a paired-end assembler for Illumina sequences that preserves the primers and inline barcodes?
illumina
barcodes
assembly
updated 2.5 years ago by
GenoMax
154k • written 2.5 years ago by
J.E.
• 0
4
votes
5
replies
2.6k
views
Forum:
I'm looking for a mentor in Bioinformatics
mentor
teaching
updated 20 months ago by
alva
• 0 • written 2.5 years ago by
cwaingartentrabajo
• 0
1
vote
1
reply
785
views
Seeking a Comprehensive Database for Genetic Background of Common Human Cell Lines
mutations
cancer
cell-line
updated 2.5 years ago by
GenoMax
154k • written 2.5 years ago by
khorms
▴ 230
0
votes
0
replies
434
views
What is the correct way to split genex_high and genex_low groups for DE analysis?
RNAseq
DESeq2
2.5 years ago by
rohanphn
• 0
0
votes
0
replies
601
views
Coriell Sample Fastq Files
Coriell
updated 2.5 years ago by
GenoMax
154k • written 2.5 years ago by
not_richard
• 0
0
votes
3
replies
1.2k
views
esearch|elink|esummary|xtract randomly skip some accession
NCBI
E-utilities
updated 2.5 years ago by
GenoMax
154k • written 2.5 years ago by
andres.firrincieli
3.9k
0
votes
0
replies
667
views
Seurat Object Manipulation
seurat
scATAC
signac
2.5 years ago by
bioinformatics.girl
▴ 30
1
vote
1
reply
1.6k
views
Difference between vcf2fq and bcftools consensus
bcftools
updated 2.5 years ago by
GenoMax
154k • written 2.5 years ago by
antoine.fauchois92
▴ 20
1
vote
1
reply
964
views
FeatureCounts tool
GFF3
FeatureCounts
annotation
updated 2.5 years ago by
Istvan Albert
103k • written 2.5 years ago by
Vikram
• 0
3
votes
9
replies
3.7k
views
fastp dedup: identical reads only?
fastq
chip-seq
updated 2.5 years ago by
Istvan Albert
103k • written 2.5 years ago by
Darked89
4.7k
1
vote
2
replies
1.1k
views
convert illumina manifest to csv
illumina
updated 2.5 years ago by
rpolicastro
13k • written 2.5 years ago by
bioguy24
▴ 230
0
votes
0
replies
591
views
suggested coverage for gene fusion detection from rna-seq data
chimera
fusion
coverage
RNA-seq
updated 2.5 years ago by
Ram
45k • written 2.5 years ago by
sigma fantasy
• 0
0
votes
1
reply
887
views
SAMtools error closing standard output: -1
bam
Samtools
updated 2.5 years ago by
Ram
45k • written 2.5 years ago by
theadrijasaha
• 0
0
votes
2
replies
1.1k
views
Annovar file
Exonic_variant
updated 2.5 years ago by
Viktor Messi
• 0 • written 3.8 years ago by
Nanditha
• 0
0
votes
1
reply
1.1k
views
Normalization method when using RnBeads to analyze MMBC (Infinium Mouse Methylation BeadChip) data
Infinium
RnBeads
MMBC
updated 2.5 years ago by
mscherer
▴ 50 • written 2.5 years ago by
ilianna
• 0
0
votes
1
reply
832
views
How do I shift the edge length of multiple trees in R?
phylogenetics
edge-length
R
updated 2.5 years ago by
Ram
45k • written 2.5 years ago by
Namenlos
• 0
0
votes
1
reply
2.3k
views
use ROSE to identify super enhancer
ROSE
Chipseq
updated 2.5 years ago by
Matthias Zepper
5.1k • written 2.5 years ago by
CL
• 0
0
votes
6
replies
2.2k
views
gatk4 download issue
gatk4
2.5 years ago by
bestone
▴ 30
0
votes
1
reply
977
views
convert PathoFact ARG output to GFF?
PathoFact
GFF
ARG
updated 2.5 years ago by
Ram
45k • written 2.5 years ago by
theadrijasaha
• 0
0
votes
1
reply
1.1k
views
Error in plot + xlab(xlab) : non-numeric argument to binary operator
scRNA
EnhancedVolcano
DESeq2
updated 2.5 years ago by
rpolicastro
13k • written 2.5 years ago by
imran
• 0
2
votes
2
replies
1.3k
views
segmentation fault error
featureCounts
updated 2.5 years ago by
Ram
45k • written 2.5 years ago by
kalyani
▴ 10
3
votes
6
replies
2.8k
views
Find Pathogenic Variants
vcf
variant-calling
2.5 years ago by
davidmaimoun
▴ 50
5
votes
6
replies
2.3k
views
DESeq2 multiple conditions, time points and sample types
DEseq2
R
edgeR
updated 2.5 years ago by
Ram
45k • written 2.5 years ago by
DHARMESH
• 0
2
votes
4
replies
1.9k
views
Is the same order when using p value or q value for compareCluster analysis?
Clusterprofiler
q-value
p-value
compareCluster
updated 2.5 years ago by
seidel
11k • written 2.5 years ago by
Lu.Lu
• 0
1
vote
3
replies
1.1k
views
Gene set enrichment analysis for genetic interactions
gsea
genetic-interactions
2.5 years ago by
rubic
▴ 270
1
vote
2
replies
1.5k
views
kinship coefficient negative in multi-sample VCF from exome sequencing
SNPs
KING
sequencing
relatedness
exome
2.5 years ago by
AMARU
• 0
1
vote
9
replies
2.4k
views
Strand non-specific bam file
RNA-Seq
Bam
updated 2.5 years ago by
Istvan Albert
103k • written 2.5 years ago by
prs
▴ 20
1
vote
1
reply
879
views
removing lines of code from a function?
python
updated 2.5 years ago by
Ram
45k • written 2.5 years ago by
zainabi8077
▴ 20
4
votes
8
replies
3.1k
views
Bowtie2: Error, fewer reads in file specified with -1 than in file specified with -2
alignment
bowtie2
updated 2.5 years ago by
GenoMax
154k • written 2.5 years ago by
zdiazmar
▴ 30
2
votes
2
replies
1.5k
views
View all rows in R studio RNASeq
RNA-Seq
RStudio
updated 2.5 years ago by
Ram
45k • written 2.5 years ago by
brandnewatthis
• 0
0
votes
3
replies
1.4k
views
In differential expression analysis using ballgown, how do we know that genes are upregulated or downregulated in control or treatment?
differential-expression-analysis
R
ballgown
updated 2.5 years ago by
ATpoint
89k • written 2.5 years ago by
Vikram
• 0
0
votes
3
replies
1.1k
views
Calculating Variant Allele Frequency
vcf
allele-frequency
updated 2.5 years ago by
Pierre Lindenbaum
166k • written 2.5 years ago by
jason
• 0
1
vote
1
reply
2.0k
views
What does Z-score and beta value mean in GWAS results?
statistics
GWAS
updated 2.5 years ago by
Jeremy Leipzig
23k • written 2.5 years ago by
Jerry
▴ 10
0
votes
1
reply
708
views
Is there any way to figure out whole gene networks in the normal tissue solely?
network
functional
gene
pathway
updated 2.5 years ago by
ATpoint
89k • written 2.5 years ago by
maximal_life
▴ 20
0
votes
2
replies
3.5k
views
How to aggregate pseudobulks: Normalization & Log-Transformation
scRNA-seq
pseudobulk
GSVA
pseudoreplicate
2.5 years ago by
Tadeoye
▴ 30
0
votes
0
replies
563
views
PathoFact GFF output
PathoFact
output
GFF
2.5 years ago by
theadrijasaha
• 0
3
votes
0
replies
767
views
How to calculate the false discovery proportion from the p-value histogram?
false-discovery-rate
2.5 years ago by
Dan
▴ 180
0
votes
2
replies
1.4k
views
GEOMX SPATIAL TRANSCRIPTOMICs
NGS
transcriptomics
ncounter
GEOMX
2.5 years ago by
Nai
▴ 50
0
votes
0
replies
465
views
Per class accuracy and 95% CI for multiclass
multinomial-regression
updated 2.5 years ago by
Ram
45k • written 2.5 years ago by
dhananya
• 0
2
votes
4
replies
1.4k
views
Unbalanced nested ANOVA in R: how to construct data frame and formulae properly?
anova
DNAseq
SNP
R
updated 2.5 years ago by
Ram
45k • written 2.5 years ago by
vvs.hazia
▴ 10
0
votes
2
replies
1.6k
views
Why is Beagle v5.4 (imputation) not giving Allele Frequencies (AF) and DR2 in my output?
qc
imputation
beagle
updated 14 months ago by
aryeesethlina5
• 0 • written 2.5 years ago by
Olivia
• 0
2
votes
5
replies
1.8k
views
How to calculate RPKM from RUVr?
RUV
R
updated 2.2 years ago by
Ram
45k • written 2.5 years ago by
star
▴ 350
0
votes
0
replies
531
views
Haploview Error
plink
Haploview
vep
2.5 years ago by
Nai
▴ 50
0
votes
0
replies
660
views
How to extract gene ID corresponding to TAIR (arabidopsis key type)? feat. enrichWP
ID
Arabidopsis
TAIR
enrichWP
gene
updated 2.5 years ago by
iraun
6.2k • written 2.5 years ago by
hellokwmin
• 0
12
votes
5
replies
6.6k
views
6 follow
Forum:
Bioinformatics opportunities in Europe?
career
updated 2.5 years ago by
alwayshope
▴ 40 • written 2.5 years ago by
melaniem
• 0
122,007 results • Page
271 of 2441
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Comment: GUI commercial software for 10x single cell gene expression analysis
Comment: How to handle TrEMBL proteins without gene annotation in plasma proteomics?
Comment: How to handle TrEMBL proteins without gene annotation in plasma proteomics?
Answer: How to handle TrEMBL proteins without gene annotation in plasma proteomics?
Comment: GUI commercial software for 10x single cell gene expression analysis
Answer: GUI commercial software for 10x single cell gene expression analysis
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I apologise for how that sounded; I wanted to be as detailed as possible.
Comment: GUI commercial software for 10x single cell gene expression analysis
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Comment: GUI commercial software for 10x single cell gene expression analysis
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Thank you but sorry, your answer sounds very AI-based...
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For a 200-SNP panel at your sample throughput, I would recommend an amplicon-based targeted sequencing approach. The workflow involves des…
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The massive difference has been reproducible across the 3 biological replicates and is in line with what we would expect in terms of the bi…
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