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121,191 results • Page
427 of 2424
Sort: Rank
Rank
Views
Votes
Replies
2
votes
1
reply
722
views
merge microarray from different platforms for differentially expressed gene analysis
merge
differential
microarray
genetic
analysis
updated 3.1 years ago by
ATpoint
88k • written 3.1 years ago by
Binghong
▴ 20
0
votes
1
reply
569
views
snpEff predicts stop_gained, but SNP wouldn't produce a stop codon
snpEff
wrong
prediction
stop_gained
updated 3.0 years ago by
Istvan Albert
102k • written 3.1 years ago by
Nadine
• 0
3
votes
5
replies
1.2k
views
technical replicates
replicates
technical
3.0 years ago by
myfam128
• 0
0
votes
0
replies
343
views
Concatenating two flowSets with overlapping sampleNames
flow
flowsets
cyto
cytometry
R
3.1 years ago by
George
• 0
1
vote
7
replies
1.9k
views
Barplot of 4 groups with p-val in R
pvalue
barplot
r
3.1 years ago by
ve9
▴ 50
2
votes
5
replies
1.3k
views
Bash command to search a fasta file for a sequence segment and to print the neighboring region of the match in every read
Bash
Match
Sequence
print
search
updated 3.0 years ago by
Michael
55k • written 3.1 years ago by
Human
• 0
1
vote
2
replies
1.6k
views
picard tools installation problems
picard-tools
collecthsmetrics
updated 23 months ago by
Ram
45k • written 3.1 years ago by
aroso491
• 0
0
votes
4
replies
1.0k
views
RNA-seq alignment in UNIX
index
sequencing
hisat2
RNA
updated 3.1 years ago by
ATpoint
88k • written 3.1 years ago by
Hien
• 0
2
votes
2
replies
769
views
IsoformSwitchAnalyzeR: object 'analysisAllIsoformsWithoutORF' not found
splicing
IsoformSwitchAnalyzeR
Alternative
3.1 years ago by
VenGeno
▴ 100
0
votes
0
replies
542
views
Job:
Nanofabrication Facility Staff Scientist
Foundry
Molecular
3.1 years ago by
BerkeleyLab
▴ 70
3
votes
1
reply
731
views
Detect outlier
outlier
Detecting
updated 3.1 years ago by
Jeremy
▴ 930 • written 3.1 years ago by
aabhordia
▴ 30
1
vote
1
reply
701
views
How to compute t-statistic
t-statistic
LDSC-SEG
updated 3.1 years ago by
Jeremy
▴ 930 • written 3.1 years ago by
zacky
▴ 10
0
votes
2
replies
764
views
near by genes for Variant
variantgene
updated 3.1 years ago by
cpad0112
21k • written 3.1 years ago by
pragathi.sneha91
• 0
2
votes
1
reply
915
views
How can I validate the results by the software package, I have recently developed using python for genomic data?
Python
analysis
scRNA-seq
software
Packages
updated 3.1 years ago by
Jeremy
▴ 930 • written 3.1 years ago by
saqlain
▴ 90
0
votes
1
reply
664
views
Advice with an Unannotated gene
genetics
genomics
variants
gene
updated 3.1 years ago by
manaswwm
▴ 570 • written 3.1 years ago by
jafisep314
• 0
2
votes
1
reply
836
views
Accessing TopMed or 1000g ancestry data (GRCh38)
ancestry
PLINK
TOPMed
GWAS
PCA
updated 3.1 years ago by
chrchang523
11k • written 3.1 years ago by
Mari
• 0
1
vote
0
replies
637
views
Herald:
The Biostar Herald for Thursday, April 28, 2022
herald
3.1 years ago by
Biostar
3.5k
3
votes
2
replies
1.3k
views
Gene ontology and GSEA
GSEA
updated 3.1 years ago by
Hamid Ghaedi
3.3k • written 3.1 years ago by
Amr
▴ 180
1
vote
6
replies
1.7k
views
Problem with adapters and taxonomy
taxonomy
adapters
kraken
updated 3.1 years ago by
Istvan Albert
102k • written 3.1 years ago by
Giulia.cosenza
▴ 110
1
vote
1
reply
963
views
Problem with the total number of variants in my .map .ped files from PLINK
PLINK
map
ped
updated 3.1 years ago by
Ram
45k • written 3.1 years ago by
elielsonveloso
• 0
5
votes
5
replies
3.4k
views
Homer makeTagDirectory does not generate the tagInfo.txt file
tagInfo.txt
Homer
HiC
Paired
data
updated 3.1 years ago by
GenoMax
151k • written 3.2 years ago by
Diana G.
▴ 30
2
votes
13
replies
2.1k
views
How to separate plasmid from whole complete genome
genebank
ncbi
updated 3.1 years ago by
GenoMax
151k • written 3.1 years ago by
Neel
▴ 20
3
votes
7
replies
1.3k
views
How to analyze the differential expression of a gene if it has several ensembl id
data
RNA-seq
DE
analysis
updated 3.1 years ago by
GenoMax
151k • written 3.1 years ago by
fuad.fsu
• 0
1
vote
1
reply
579
views
Pathogenicity prediction experiment
VEP
VCF
ensembl
pathogenicity
3.1 years ago by
Newbie
• 0
1
vote
2
replies
800
views
Building an extended PPI network in Cytoscape without BisoGenet
PPI
network
Cytoscape
3.1 years ago by
amir.rakhimov.b
• 0
3
votes
5
replies
2.0k
views
Getting Uniprot IDs of a set of Genes
UniprotKB
ID_mapping
updated 3.0 years ago by
Elisabeth Gasteiger
★ 2.4k • written 3.1 years ago by
GenesisBio
• 0
2
votes
4
replies
2.1k
views
whatsHap didn't phase all variants
whatsHap
phasing
updated 3.1 years ago by
bouchenak.chuxi
• 0 • written 4.0 years ago by
s2004341
• 0
0
votes
1
reply
1.2k
views
Jellyfish for Paired End Reads
k-mer
fastq
Jellyfish
counting
fasta
updated 3.1 years ago by
GenoMax
151k • written 3.1 years ago by
hpalk42
• 0
1
vote
1
reply
1.1k
views
phasing VCF files with missing genotype
Phasing
updated 3.1 years ago by
bouchenak.chuxi
• 0 • written 3.5 years ago by
summerday1112
▴ 10
0
votes
0
replies
1.1k
views
Job:
Tenure Track Assistant Professor or Associate Professor of Biostatistics at Department of Public Health, Aarhus University
Health
Biostatistics
Public
statistics
theoretical
3.1 years ago by
info
▴ 80
3
votes
11
replies
2.3k
views
Help with massive SRA download of mixed file types (SE fastq, PE fastq, bam)
sra-toolkit
faster-dump
SRA
updated 3.1 years ago by
jared.andrews07
★ 18k • written 3.1 years ago by
jmnz22
▴ 10
2
votes
1
reply
1.2k
views
Job:
Junior bioinformatician in italy
Italy
updated 2.9 years ago by
Ram
45k • written 3.1 years ago by
Giulia.cosenza
▴ 110
0
votes
3
replies
1.9k
views
Cutadapt issues when running nfcore pipeline
methylseq
trimgalore
cutadapt
nfcore
updated 3.1 years ago by
Matthias Zepper
5.1k • written 3.1 years ago by
aroso491
• 0
1
vote
1
reply
638
views
WGCNA - plotMat colors - how to change from RedGreen
WGCNA
updated 3.1 years ago by
andres.firrincieli
3.9k • written 3.1 years ago by
annamariabugaj
• 0
1
vote
0
replies
553
views
Relatedness with KING vs heterogeneous data
relatedness
3.1 years ago by
German.M.Demidov
★ 3.0k
0
votes
0
replies
479
views
Fake indels and artificially low coverage in bcftools mpileup when using close references
snp
samtools
bcftools
mpileup
updated 23 months ago by
Ram
45k • written 3.1 years ago by
alnam
▴ 10
7
votes
5
replies
2.9k
views
what is the benefit of the de bruijn algorithm for short read assembly?
Assembly
de Bruijn algorithm
K-mer
updated 3.1 years ago by
Michael
55k • written 8.6 years ago by
seta
★ 1.9k
0
votes
3
replies
2.4k
views
How to get a pdb of the second chain of a homodimer using VMD?
vmd
updated 3.1 years ago by
Jiyao Wang
▴ 380 • written 10.2 years ago by
mcleodcmm
• 0
0
votes
4
replies
3.7k
views
Is there any easy way to get ASA/RSA for the whole PDB?
pdb
asa
protein
updated 3.1 years ago by
Jiyao Wang
▴ 380 • written 10.2 years ago by
ajingnk
▴ 130
3
votes
5
replies
1.7k
views
[E::bwa_idx_load_from_disk] fail to locate the index files
alignment
BWA
3.1 years ago by
melissachua90
▴ 70
3
votes
2
replies
864
views
Tools for finding a walk in a De Bruijn graph
assembly
dbsp
debruijn
updated 3.1 years ago by
Matthias Zepper
5.1k • written 3.1 years ago by
Roman
▴ 20
1
vote
2
replies
1.0k
views
Error The tag ING/CSQ not found in the header using bcftools
vcf
bcftools
3.1 years ago by
Manuel
▴ 50
8
votes
3
replies
1.2k
views
MultiQC output shows that data processing steps are ineffective
FastQC
trimming
updated 2.0 years ago by
Ram
45k • written 3.1 years ago by
melissachua90
▴ 70
1
vote
4
replies
1.1k
views
Two rounds of batch effect removal
DESeq2
removeBatchEffect
3.1 years ago by
Kazuna
• 0
4
votes
3
replies
1.1k
views
PAINS
PAINS
updated 3.1 years ago by
GenoMax
151k • written 3.1 years ago by
Safah
• 0
1
vote
3
replies
962
views
How to obtain genomic coordinates of novel transcripts?
ensembldb
r
updated 3.1 years ago by
ATpoint
88k • written 3.1 years ago by
nattzy94
▴ 60
0
votes
3
replies
1.3k
views
miRNA-seq alignment bowtie2
hisat2
alignment
miRNA-seq
bowtie2
3.0 years ago by
imaparna27
▴ 20
0
votes
2
replies
875
views
Adding RNA-seq data to machine learning
machine
learning
3.1 years ago by
hafiz.talhamalik
▴ 350
3
votes
4
replies
1.1k
views
Extract 16S rRNA gene from GenBank files?
NCBI
16S
3.1 years ago by
MSRS
▴ 590
0
votes
2
replies
1.5k
views
Remove polymorphic SNPs from VCF file
SNP
updated 3.1 years ago by
meimingwu
• 0 • written 5.0 years ago by
goatsrunfaster
▴ 60
121,191 results • Page
427 of 2424
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Comment: Analysing Problem Seen In MEGA X
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I'm also facing the same issue. Have you been able to find a way to fix it?
Comment: How to visualize Combat-seq corrected counts
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Sorry, I accidentally used ComBat! ComBat-seq did not produce negative counts. Thanks for all the help!
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Yes, I have tested all of them. I guess NCBI does not have this particular strain.
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As with any visualisation method, there is a time and a place for them. They are often misused, or used when a different method would be be…
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There is no answer to this. Some people will say 10, other 3, others 500. Generally, since single-cell is noisy and has dropouts, even for …
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Please use `ADD REPLY/ADD COMMENT` when responding to existing posts. `ADD ANSWER` is only for new answers to original question.
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...I decided to try 'ComplexHeatmap' : ```r ha = HeatmapAnnotation(df = annot_col, which="column",show_annotation_name = FALSE,show_legend=…
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