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1,000 results • Page
5 of 20
Sort: replies
Rank
Views
Votes
Replies
10
votes
15
replies
6.2k
views
DIAMOND blast imported into MEGAN6 has no taxonomic assignment
blast
MEGAN6
Taxonomy
DIAMOND
7.5 years ago by
Farbod
★ 3.4k
7
votes
15
replies
4.3k
views
Biopython Pairwise Alignment output
biopython
needleman
global alignment
4.1 years ago by
tommaso.green
• 0
1
vote
15
replies
4.4k
views
Ultrafast alignment of short sequences to a genome (with up to 5 mismatches!)
genome
alignment
updated 2.4 years ago by
Ram
43k • written 9.7 years ago by
Aurelie MLB
▴ 360
3
votes
15
replies
2.1k
views
Overlapping regions in a BED file
regions
BED
Sequence
exons
annotation
22 months ago by
Matej
• 0
7
votes
15
replies
7.2k
views
6 follow
blastn error - NCBI C++ Exception
assembly
blast
alignment
updated 2.1 years ago by
lieven.sterck
15k • written 3.1 years ago by
sunnykevin97
▴ 980
6
votes
15
replies
1.6k
views
Reads partly within an exon
RNA-Seq
6.8 years ago by
benjyrolls
▴ 70
5
votes
15
replies
5.4k
views
Annotation with snpEFF
annotation
vcf
snpeff
extractFields
updated 5.9 years ago by
Biostar
20 • written 5.9 years ago by
NB
▴ 960
8
votes
15
replies
2.0k
views
RNAseq differential expression analysis : no significative FDR but significative GO enrichment
RNA-Seq
differential expression
4.6 years ago by
guillaume.rbt
★ 1.0k
0
votes
15
replies
3.2k
views
SAMFormatException: Did not inflate expected amount error
WES
updated 2.5 years ago by
greekkey
▴ 20 • written 2.9 years ago by
smrutimayipanda
▴ 20
2
votes
15
replies
4.2k
views
How to interpret reads mapped to genome from samtools flagstat vs TopHat align_summary.txt ?
RNA-Seq
8.1 years ago by
Vasu
▴ 770
1
vote
15
replies
3.3k
views
How to perform multiple alignment using MAFFT?
genome
alignment
gene
sequence
3.1 years ago by
anikcropscience
▴ 230
2
votes
15
replies
2.2k
views
to get each covariate with PC loading in PCA
RNA-seq
PCA
5.3 years ago by
Grace_G
▴ 20
2
votes
15
replies
4.1k
views
Bowtie2 error :: (ERR): bowtie2-align died with signal 6 (ABRT) (core dumped)
next-gen
SNP
alignment
updated 4.1 years ago by
wm
▴ 560 • written 4.1 years ago by
shrutidabral
▴ 10
4
votes
15
replies
4.0k
views
Paired-read alignment length from BAM/SAM file
bam
sam
paired-read
alignment
6.9 years ago by
Soumitra Pal
▴ 10
5
votes
15
replies
1.6k
views
NGS Sequencing depths
next-gen
sequencing
gene
7.2 years ago by
sliproach
▴ 10
3
votes
15
replies
3.2k
views
Less and less genes predicted with each iteration of SNAP/MAKER
maker
annotation
snap
gene prediction
genomics
updated 2.7 years ago by
jaredbernard
▴ 30 • written 4.1 years ago by
mrmrwinter
▴ 30
1
vote
15
replies
2.0k
views
Samtools merge Illumina and PB bam file empty
Illumina
samtools
Bam
PacBio
updated 13 months ago by
Ram
43k • written 3.8 years ago by
talbots
▴ 30
1
vote
15
replies
6.0k
views
How to Extract Specific Region on Bam file
Nanopore
HG38
Rna-Seq
Genome
updated 2.9 years ago by
Kevin Blighe
88k • written 2.9 years ago by
santos48
▴ 40
9
votes
15
replies
1.3k
views
Construction of single sequence assembly out of contigs
Contigs
Bacteria
Genome
WGS
5 months ago by
analyst
▴ 50
6
votes
15
replies
2.7k
views
Why can't I reproduce the same heat map
ggplots
R
RNA-Seq
updated 5.8 years ago by
Biostar
20 • written 5.9 years ago by
Za
▴ 140
10
votes
15
replies
6.2k
views
convert fasta/gb to vcf
fasta
vcf
genbank
gff
updated 13 months ago by
Ram
43k • written 5.6 years ago by
marongiu.luigi
▴ 710
20
votes
15
replies
30k
views
8 follow
Converting SNP from chr:pos to rs number using PLINK?
plink
SNP
updated 21 months ago by
Ram
43k • written 8.4 years ago by
dam4l
▴ 200
7
votes
15
replies
2.2k
views
very low coverage when mappin genomic DNA
mapping
coverage
DNA
genomic
updated 2.7 years ago by
ATpoint
82k • written 2.7 years ago by
Lila M
★ 1.2k
2
votes
15
replies
1.6k
views
How to call all the allele in samples
SNP
6.1 years ago by
Kritika
▴ 260
1
vote
15
replies
3.7k
views
Install Lefse in Ubuntu 12
install
lefse
microbiome
5.9 years ago by
goh
▴ 10
5
votes
15
replies
1.9k
views
Testing uniform distribution of SNPs across chromosome
uniform
vcf
SNP
5.0 years ago by
misterie
▴ 110
1
vote
15
replies
2.8k
views
Copy Number Analysis on single file
CNV
updated 4.7 years ago by
Kevin Blighe
88k • written 4.7 years ago by
user31888
▴ 130
3
votes
15
replies
5.6k
views
Pairwise sequence alignment with Biojava?
sequence-alignment
biojava
java
updated 2.3 years ago by
Ram
43k • written 9.5 years ago by
Bioaln
▴ 360
5
votes
15
replies
1.5k
views
Get list of gene signatures published
bailey
genes
subtype
pancreas
3.3 years ago by
sabin
▴ 50
2
votes
15
replies
1.2k
views
Manipulate refseq database
ncbi
database
nt
refseq
updated 4.3 years ago by
Biostar
20 • written 4.3 years ago by
anasofiamoreira94
▴ 80
11
votes
15
replies
2.9k
views
How do I get the read counts for a specific exon
bam
exon
updated 6.1 years ago by
Ram
43k • written 6.1 years ago by
b10hazard
▴ 30
1
vote
15
replies
3.7k
views
Can I use PICARD (SortSam) instead of SAMTOOLS (sort) for sorting bam files in RNAseq pipeline where HISAT2 is used for alignment.
RNA-Seq
software error
sequencing
next-gen
6.0 years ago by
shuksi1984
▴ 60
0
votes
15
replies
2.2k
views
Chromosome accession numbers correspond to which chromosome?
bam
chromosome
bed
18 months ago by
amy__
▴ 160
1
vote
14
replies
3.8k
views
Picard MarkDuplicates shows error (removing pcr duplicates)
snp
alignment
sequence
updated 5.5 years ago by
Kevin Blighe
88k • written 5.5 years ago by
ashaneev07
▴ 20
4
votes
14
replies
3.6k
views
6 follow
Cutadapt installation - user defined directory
cutadapt Installation
5.8 years ago by
davide.chiarugi
▴ 20
15
votes
14
replies
3.2k
views
Penalty model of BWA MEM and BOWTIE2?
RNA-Seq
bwa mem
bowtie2
alignment
6.3 years ago by
John
▴ 270
5
votes
14
replies
2.0k
views
Fastqc genome reads
genome
fastqc
updated 2.3 years ago by
ATpoint
82k • written 2.3 years ago by
Ak
▴ 60
4
votes
14
replies
1.2k
views
remove white space in fastq file
fastq
updated 4 months ago by
GenoMax
142k • written 4 months ago by
gkarere
• 0
4
votes
14
replies
3.2k
views
Variance decomposition analysis (solved)
RNA-Seq
R
hypothesis-test
updated 2.3 years ago by
Ram
43k • written 9.6 years ago by
juncheng
▴ 220
1
vote
14
replies
2.0k
views
Can't Make Sense Of Gene Symbols
gene symbol
gene ontology
entrez
myGene
python
5.7 years ago by
sinifdosyalari12h
▴ 20
2
votes
14
replies
6.0k
views
Identifying UMIs from fastq files
sequencing
miRNA seq
6.0 years ago by
hothriananya
▴ 70
1
vote
14
replies
4.3k
views
RNAseq: What is the difference between the units log2 (tpm + 0.001) and log2 (norm_count + 1)
IsoPct
units
RNAseq
3.0 years ago by
muet-10
• 0
8
votes
14
replies
2.5k
views
6 follow
kallisto pseudoalignment rate is lower than literature
pseudoalignment
kallisto
RNA-seq
2.8 years ago by
johnsonqinz
• 0
8
votes
14
replies
6.0k
views
Error in BWA-MEM running in linux
RNA-Seq
BWA-MEM
alignment
updated 6.0 years ago by
GenoMax
142k • written 6.0 years ago by
modarzi
▴ 170
2
votes
14
replies
1.6k
views
VCF2MAF structural variant file issue.
VCF2MAF
updated 9 months ago by
Ram
43k • written 9 months ago by
The_PyPanda
▴ 10
3
votes
14
replies
1.6k
views
How to extract just the reads ID, start position and lenght from the alliigned file?
next-gen
sequencing
updated 5.8 years ago by
ATpoint
82k • written 5.8 years ago by
vellryba
• 0
0
votes
14
replies
2.3k
views
how to identify protein protein interactions
proteomics
7.9 years ago by
Learner
▴ 280
1
vote
14
replies
3.6k
views
Cuffmerge error(?) for RNA-seq
RNA-Seq
updated 3.3 years ago by
bioinfonewbie
• 0 • written 6.3 years ago by
bioinfo
▴ 10
5
votes
14
replies
8.0k
views
Microrna Adapter Trimming
updated 10.4 years ago by
Fabio Marroni
★ 3.0k • written 10.5 years ago by
xiaojuhu13
▴ 150
2
votes
14
replies
2.5k
views
grep command for fasta header
fasta
2.6 years ago by
harry
▴ 30
1,000 results • Page
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Comment: How to calculate coverage of Nanopore long read data?
by
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Thank you! I eventually used the information generated by three tools (samtools coverage+ mosdepth + NanoPlot).
Comment: Alphaphold 3 pLDDT coloring scheme in chimerax?
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Please accept your own answer to mark the post as solved.
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The simple answer is to plot it natively with plotly rather than use `ggplotly`. See [this stackoverflow answer](https://stackoverflow.com/…
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