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Merging multiple runs of the same samples
metaspades fastq Megahit shotgun metagenomics sequencing
updated 7 months ago by 152k • written 7 months ago by ▴ 90
0
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1
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802
views
WGCNA: minModuleSize is not responding correctly
RNA-Seq WGCNA
updated 2.6 years ago by 3.9k • written 2.6 years ago by ▴ 90
0
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1
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2.8k
views
Comment: Comment: error while plot data with deSeq2
3.6 years ago by bioinformaticssrm2011 ▴ 90
0
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1
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2.8k
views
Comment: Comment: error while plot data with deSeq2
3.6 years ago by bioinformaticssrm2011 ▴ 90
0
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0
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2.8k
views
Comment: Comment: error while plot data with deSeq2
3.6 years ago by bioinformaticssrm2011 ▴ 90
0
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1
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2.8k
views
Comment: Comment: error while plot data with deSeq2
3.6 years ago by bioinformaticssrm2011 ▴ 90
1
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9
replies
2.8k
views
error while plot data with deSeq2
DESeq2 RNA-Seq
updated 3.6 years ago by 15k • written 3.6 years ago by ▴ 90
1
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0
replies
8.8k
views
Comment: A: List of bioinformatics journal with imapact factor around 1 and no publication f
updated 5.4 years ago by 45k • written 10.6 years ago by ▴ 90
0
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1
reply
6.6k
views
Comment: C: Fungal genome annotation
updated 5.7 years ago by 45k • written 10.3 years ago by ▴ 90
1
vote
1
reply
6.6k
views
Comment: C: Fungal genome annotation
updated 5.7 years ago by 45k • written 10.3 years ago by ▴ 90
6
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4
replies
11k
views
tree obtained from neighbor-joining and maximum-likelihood are different.
sequence alignment
updated 3.4 years ago by 45k • written 10.6 years ago by ▴ 90
6
votes
19
replies
15k
views
6 follow
Using trimmomatic on multiple paired-end read files
ngs Assembly genome next-gen sequencing
updated 6.1 years ago by 5.9k • written 8.3 years ago by ▴ 90
1
vote
0
replies
13k
views
Comment: C: Linux for loop for 2 inputs and 4 outputs for Trimmomatic fastq quality trimming
8.3 years ago by bioinformaticssrm2011 ▴ 90
1
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1
reply
15k
views
Comment: C: Using trimmomatic on multiple paired-end read files
8.3 years ago by bioinformaticssrm2011 ▴ 90
0
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1
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15k
views
Comment: C: Using trimmomatic on multiple paired-end read files
8.3 years ago by bioinformaticssrm2011 ▴ 90
0
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1
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15k
views
Comment: C: Using trimmomatic on multiple paired-end read files
8.3 years ago by bioinformaticssrm2011 ▴ 90
7
votes
9
replies
5.5k
views
rename mutiple fasta header for mutiple fasta files
genome next-gen sequencing sequence
updated 8.3 years ago by 8.7k • written 8.3 years ago by ▴ 90
0
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1
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15k
views
Comment: C: Using trimmomatic on multiple paired-end read files
8.3 years ago by bioinformaticssrm2011 ▴ 90
0
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1
reply
15k
views
Comment: C: Using trimmomatic on multiple paired-end read files
8.3 years ago by bioinformaticssrm2011 ▴ 90
0
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0
replies
5.5k
views
Comment: C: rename mutiple fasta header for mutiple fasta files
8.3 years ago by bioinformaticssrm2011 ▴ 90
0
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0
replies
5.5k
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Comment: C: rename mutiple fasta header for mutiple fasta files
8.3 years ago by bioinformaticssrm2011 ▴ 90
0
votes
1
reply
2.2k
views
Result interpretation of ibda-hybrid tool for assembly.
Assembly genome next-gen alignment sequencing
updated 8.7 years ago by 48k • written 8.7 years ago by ▴ 90
1
vote
5
replies
5.7k
views
PAN and CORE genome analysis
genome sequencing next-gen Assembly
updated 3.0 years ago by 45k • written 10.2 years ago by ▴ 90
4
votes
9
replies
8.8k
views
List of bioinformatics journal with imapact factor around 1 and no publication fee
sequence
2.6 years ago by bioinformaticssrm2011 ▴ 90
6
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10
replies
8.7k
views
6 follow
transcription factor binding site prediction software/server
sequence genome-sequencing
2.6 years ago by bioinformaticssrm2011 ▴ 90
0
votes
1
reply
4.4k
views
Comment: Comment: python script for deleting basepair in fasta format
updated 3.5 years ago by 45k • written 9.9 years ago by ▴ 90
0
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0
replies
2.8k
views
Comment: Comment: Protein sequence analysis
updated 2.4 years ago by 45k • written 10.1 years ago by ▴ 90
6
votes
4
replies
2.8k
views
Protein sequence analysis
alignment blast
updated 2.4 years ago by 45k • written 10.1 years ago by ▴ 90
0
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0
replies
6.5k
views
Comment: Comment: How to get the abundance of genes in metagenomes from MG RAST
updated 2.4 years ago by 45k • written 10.1 years ago by ▴ 90
0
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1
reply
5.7k
views
Comment: Comment: PAN and CORE genome analysis
updated 3.6 years ago by 45k • written 10.2 years ago by ▴ 90
0
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0
replies
8.3k
views
Comment: Comment: Augustus result interpretation
updated 3.1 years ago by 45k • written 10.3 years ago by ▴ 90
1
vote
2
replies
8.3k
views
Augustus result interpretation
gene-sequence genome-sequencing
updated 3.1 years ago by 45k • written 10.3 years ago by ▴ 90
0
votes
2
replies
8.7k
views
Comment: Comment: transcription factor binding site prediction software/server
2.6 years ago by bioinformaticssrm2011 ▴ 90
0
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1
reply
8.7k
views
Comment: Comment: transcription factor binding site prediction software/server
updated 3.1 years ago by 45k • written 10.3 years ago by ▴ 90
0
votes
0
replies
8.7k
views
Comment: Comment: transcription factor binding site prediction software/server
updated 3.1 years ago by 45k • written 10.3 years ago by ▴ 90
3
votes
6
replies
7.2k
views
MAKER genome annotation installation help
software-error genome maker
updated 3.2 years ago by 45k • written 10.4 years ago by ▴ 90
0
votes
0
replies
13k
views
Comment: Comment: Tophat Installation On Ubuntu 11.10 Server
updated 3.2 years ago by 45k • written 10.3 years ago by ▴ 90
4
votes
6
replies
6.6k
views
Tool: Fungal genome annotation
genome sequencing
updated 3.5 years ago by 45k • written 10.4 years ago by ▴ 90
0
votes
0
replies
7.2k
views
Comment: Comment: MAKER genome annotation installation help
updated 3.2 years ago by 45k • written 10.4 years ago by ▴ 90
0
votes
1
reply
7.2k
views
Comment: Comment: MAKER genome annotation installation help
updated 3.2 years ago by 45k • written 10.4 years ago by ▴ 90
0
votes
0
replies
7.2k
views
Comment: Comment: MAKER genome annotation installation help
updated 3.2 years ago by 45k • written 10.4 years ago by ▴ 90
0
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1
reply
3.3k
views
Comment: Comment: I have 10 closely related sequence, and i want to create a common primer for tha
updated 3.3 years ago by 45k • written 10.6 years ago by ▴ 90
2
votes
5
replies
3.3k
views
I have 10 closely related sequence, and I want to create a common primer for that, how can I create common primer ?
sequence genome-sequencing
updated 3.3 years ago by 45k • written 10.6 years ago by ▴ 90
0
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1
reply
3.3k
views
Comment: Comment: I have 10 closely related sequence, and i want to create a common primer for tha
updated 3.3 years ago by 45k • written 10.6 years ago by ▴ 90
0
votes
0
replies
11k
views
Comment: Comment: tree obtained from neighbor-joining and maximum-likelihood are different.
updated 3.4 years ago by 45k • written 10.6 years ago by ▴ 90
0
votes
0
replies
11k
views
Comment: Comment: tree obtained from neighbor-joining and maximum-likelihood are different.
updated 3.4 years ago by 45k • written 10.6 years ago by ▴ 90
0
votes
0
replies
4.4k
views
Comment: C: python script for deleting basepair in fasta format
10.9 years ago by bioinformaticssrm2011 ▴ 90
8
votes
17
replies
4.4k
views
python script for deleting basepair in fasta format
sequence python
updated 3.5 years ago by 45k • written 10.9 years ago by ▴ 90
0
votes
1
reply
4.4k
views
Comment: Comment: python script for deleting basepair in fasta format
updated 3.5 years ago by 45k • written 10.9 years ago by ▴ 90
0
votes
1
reply
4.4k
views
Comment: Comment: python script for deleting basepair in fasta format
updated 3.5 years ago by 45k • written 10.9 years ago by ▴ 90
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