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1,000 results • Page
2 of 20
Sort: Views
Rank
Views
Votes
Replies
2
votes
4
replies
12k
views
Run BLAST on Linux terminal
ncbi
nBLAST
linux
blast
updated 15 months ago by
Ram
41k • written 8.2 years ago by
Abdul Rafay Khan
★ 1.2k
0
votes
3
replies
12k
views
edgeR: likelihood ratio test or quasi-likelihood F-test?
R
rna-seq
next-gen
6.7 years ago by
moxu
▴ 510
4
votes
9
replies
12k
views
Seqtk subseq: structure of file name.lst
sequence
next-gen
updated 5.6 years ago by
Ram
41k • written 5.6 years ago by
ste.lu
▴ 80
0
votes
1
reply
12k
views
PLINK 1.9 - Converting PED/MAP to BED/BIM/FAM with missing values
plink
updated 7.4 years ago by
Biostar
20 • written 7.4 years ago by
rednalf
▴ 90
2
votes
13
replies
12k
views
8 follow
(ERR): bowtie2-align exited with value 1
software error
RNA-Seq
updated 5.9 years ago by
basucsmcri
• 0 • written 6.8 years ago by
biostarsb
▴ 30
3
votes
2
replies
12k
views
ExAC PLI score calculation
DNA-Seq
6.8 years ago by
jonessara770
▴ 240
7
votes
9
replies
12k
views
Different alignment rates for Hisat2 and STAR, Hisat2 has lower alignment rate and STAR have many multi aligned reads
RNA-Seq
updated 6.2 years ago by
Satyajeet Khare
★ 1.6k • written 6.2 years ago by
SMILE
▴ 170
8
votes
5
replies
12k
views
samtools tview symbols
samtools
updated 13 months ago by
Ram
41k • written 8.4 years ago by
biolab
★ 1.4k
0
votes
3
replies
12k
views
Extracting Specific Columns from Multiple Files & Writing to File Python
python
file-handeling
7.6 years ago by
BioICoder
▴ 40
41
votes
55
replies
11k
views
6 follow
hash function for DNA sequences
hash
hashing
DNA
7.7 years ago by
midox
▴ 290
3
votes
8
replies
11k
views
6 follow
How do I go from UniProt ID to retrieving the gene name?
sequence
6.1 years ago by
a.rex
▴ 350
1
vote
13
replies
11k
views
MarkDuplicates memory issue
alignment
Picard
MarkDuplicates
7.9 years ago by
cacampbell
▴ 50
15
votes
6
replies
11k
views
6 follow
MAF vs VAF
sequencing
5.7 years ago by
lauren.wahyudi
▴ 50
0
votes
4
replies
11k
views
Convert .gbf file to .gbk or .gff
gbk
gff
gbf
updated 10 months ago by
Ram
41k • written 8.6 years ago by
che.bellaj
• 0
2
votes
3
replies
11k
views
converting maf to vcf
Exome
maf2vcf
updated 10 months ago by
Ram
41k • written 8.6 years ago by
ashishchahl
• 0
4
votes
7
replies
11k
views
Grab Coordinate Of Centromeres From Ucsc
ucsc
10.6 years ago by
jeansimon32
▴ 170
6
votes
7
replies
11k
views
bedtools intersect bed and vcf, coordinates problem
bedtools
bed
vcf
6.7 years ago by
abascalfederico
★ 1.2k
3
votes
4
replies
11k
views
Zlib.Error: -3 While Decompressing: Invalid Distance To Far Back (By Using Macs For Chip-Seq Data)
error
12.2 years ago by
Lisanne
• 0
1
vote
2
replies
11k
views
Downloading BAM files GEO/SRA
bam
sra
geo
samtools
sratoolkit
7.4 years ago by
ilobelo
▴ 10
3
votes
16
replies
11k
views
combining z-scores into a single z-score value
excel
R
statistics
updated 6 months ago by
Ram
41k • written 4.7 years ago by
Star
▴ 60
3
votes
4
replies
11k
views
basename: missing operand
snp
4.4 years ago by
evelyn
▴ 220
2
votes
8
replies
11k
views
Loading Custom Genome In Igv Is Not Displaying Genes, Names Match.
igv
gff
reference
contigs
11.8 years ago by
Nickengland
▴ 130
4
votes
14
replies
11k
views
All the reads aligned using STAR have low mapping quality (0-3). What is happening?
mapping quality
STAR
BWA
alignment
7.4 years ago by
kirannbishwa01
★ 1.6k
2
votes
4
replies
11k
views
Pymol-Generate Pymol Movie To Mpeg
pymol
updated 22 months ago by
Ram
41k • written 11.9 years ago by
Reyhaneh
▴ 530
2
votes
0
replies
10k
views
How to plot UniFrac PCoA with 95% confidence Elipses in R
metagenomics
ordiellipse
vegan
R
phyloseq
updated 20 months ago by
Ram
41k • written 8.9 years ago by
c.v.oflynn
▴ 100
3
votes
1
reply
10k
views
Negative P-Values
gene
genome
next-gen-sequencing
updated 15 months ago by
Ram
41k • written 8.3 years ago by
stevenlang123
▴ 200
7
votes
8
replies
10k
views
Picard tools duplicate removal
RNA-Seq
picard-tools
6.1 years ago by
blur
▴ 280
5
votes
9
replies
10k
views
Error with samtools faidx...Different line length in sequence
samtools
faidx
updated 5.5 years ago by
Biostar
20 • written 5.7 years ago by
oars
▴ 200
2
votes
1
reply
10k
views
Calculate Linkage Disequilibrium For Snps (Using R^2)
snp
linkage
10.4 years ago by
TitoPullo
▴ 180
3
votes
2
replies
10k
views
BWA-MEM Vs BWA-ALN
next-gen
genome
alignment
7.6 years ago by
SOHAIL
▴ 400
11
votes
10
replies
10k
views
Extracting from tophat outputs reads pairs and splice-junctions with a single best match
TOPHAT
RNA-Seq
updated 23 months ago by
Ram
41k • written 9.3 years ago by
trakhtenberg
▴ 160
2
votes
2
replies
10k
views
How to make clusters in heat map using ggplot2?
RNA-Seq
rna-seq
R
4.6 years ago by
John
▴ 270
1
vote
2
replies
10k
views
Converting MSTRG from stringtie with gene name
RNA-Seq
Stringtie
updated 5.9 years ago by
Biostar
20 • written 5.9 years ago by
fhassanz
▴ 20
0
votes
1
reply
10k
views
Is it normal that nearly all of p-value is equal to 0.1 in PERMANOVA analysis
PERMANOVA
statistics
metagenomics
updated 3.0 years ago by
dqq102829
• 0 • written 3.9 years ago by
zhangdengwei
▴ 210
3
votes
6
replies
10k
views
6 follow
How to calculate genetic correlation with R
R
updated 19 months ago by
ibomsolomon
• 0 • written 9.6 years ago by
Tohamy
▴ 80
13
votes
22
replies
10k
views
SVA : Setting up the data from an ExpressionSet and applying sva function to extimate batches
sva
combat
batch effects
updated 6.2 years ago by
Biostar
20 • written 6.4 years ago by
lessismore
★ 1.3k
0
votes
0
replies
10k
views
Map Between Uniprot Accesion And Gene.Symbol Using R Or/And Mysql
r
bioconductor
mysql
9.9 years ago by
jfertaj
▴ 110
0
votes
0
replies
10k
views
pheatmap row annotation and title font size questions
heatmap
pheatmap
updated 11 months ago by
Ram
41k • written 8.5 years ago by
neokao
• 0
7
votes
9
replies
10.0k
views
Samtools Index Segmentation Fault
samtools
index
9.7 years ago by
Noushin N
▴ 600
1
vote
1
reply
10.0k
views
Raxml bootstrap support values
figtree
raxml
bootstrap
updated 2.2 years ago by
Ram
41k • written 9.6 years ago by
JackBel
• 0
1
vote
5
replies
9.9k
views
What Agilent Interval Files (.Bed) Should I Use For Exome Variant Calling With Gatk?
bed
agilent
gatk
updated 3.8 years ago by
Karma
▴ 310 • written 10.0 years ago by
newDNASeqer
▴ 750
2
votes
16
replies
9.9k
views
Tophat with Bowtie2 long index
tophat
bowtie
updated 23 months ago by
Ram
41k • written 9.4 years ago by
BDK_compbio
▴ 140
2
votes
8
replies
9.8k
views
Size of typical genomic data
genomic
updated 8 months ago by
Ram
41k • written 5.6 years ago by
Nicolas Rosewick
10k
6
votes
3
replies
9.8k
views
Sequence duplication levels-RNA Seq
RNA-Seq
updated 3.2 years ago by
joshua.theisen
▴ 30 • written 5.7 years ago by
makwana.kd
▴ 50
3
votes
3
replies
9.7k
views
bcftools mpileup output format
bcftools
mpileup
5.3 years ago by
tarek.mohamed
▴ 350
3
votes
4
replies
9.7k
views
Aligning RNA seq data to genome or transcriptome
RNA-Seq
ngs
transcriptome
genome
updated 6.2 years ago by
Ram
41k • written 6.2 years ago by
KVC_bioinfo
▴ 590
3
votes
10
replies
9.6k
views
How can I obtain SNP from TCGA?
Risky-allele
BRCA
SNP
updated 23 months ago by
Ram
41k • written 9.2 years ago by
purmod
▴ 10
0
votes
2
replies
9.6k
views
DESeq2 pheatmap returns Error in check.length("fill") : 'gpar' element 'fill' must not be length 0
RNA-Seq
DESeq2
gpar
pheatmap
6.1 years ago by
Anthony.Knox
▴ 60
0
votes
8
replies
9.5k
views
how to find a read by name in a bam file
next-gen-sequencing
updated 5 months ago by
Ram
41k • written 6.4 years ago by
himanimalhotra89
• 0
6
votes
8
replies
9.5k
views
7 follow
Converting SNP names from Illumina GSA array to rsID using PLINK
SNP
plink
6.2 years ago by
dam4l
▴ 200
1,000 results • Page
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C: Recommended cutoff for FDR - 0.05 or 0.1
A: Recommended cutoff for FDR - 0.05 or 0.1
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