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3
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564
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Comparing two sets of 16s sequences to identify any identicle (within 97%) sequences
alignment genome
updated 4.1 years ago by ★ 27k • written 4.1 years ago by ▴ 80
0
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0
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2.4k
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Comment: C: BUSCO vs CheckM, which is best for determining bacterial genome completness.
4.1 years ago by robert.murphy ▴ 80
5
votes
2
replies
2.4k
views
BUSCO vs CheckM, which is best for determining bacterial genome completness.
genome
updated 4.1 years ago by ★ 27k • written 4.1 years ago by ▴ 80
1
vote
6
replies
4.3k
views
How to convert gff to gbk format. I have the assembled fasta also
genome
updated 4.1 years ago by 20 • written 4.3 years ago by ▴ 80
0
votes
1
reply
856
views
Can I do a GO enrichment analysis with bacterial species abundance instead of expression values?
genome
updated 4.2 years ago by 20 • written 4.3 years ago by ▴ 80
0
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2
replies
2.5k
views
Comment: C: Scanpy vs DeSeq for single cell RNASeq DE gene analysis
4.2 years ago by robert.murphy ▴ 80
0
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0
replies
4.3k
views
Comment: C: How to convert gff to gbk format. I have the assembled fasta also
4.3 years ago by robert.murphy ▴ 80
0
votes
1
reply
4.3k
views
Comment: C: How to convert gff to gbk format. I have the assembled fasta also
4.3 years ago by robert.murphy ▴ 80
0
votes
1
reply
4.3k
views
Comment: C: How to convert gff to gbk format. I have the assembled fasta also
4.3 years ago by robert.murphy ▴ 80
0
votes
1
reply
847
views
Convert gene sequence into protein sequence them HMM
alignment genome
updated 4.3 years ago by ▴ 1000 • written 4.3 years ago by ▴ 80
0
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0
replies
912
views
Comment: C: Cross referencing biosynthetic gene clusters in metagenome, best way to do this?
4.3 years ago by robert.murphy ▴ 80
0
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1
reply
1.5k
views
Comment: C: Can I use deseq on non transcriptome data?
4.3 years ago by robert.murphy ▴ 80
1
vote
1
reply
1.5k
views
Comment: C: Can I use deseq on non transcriptome data?
4.3 years ago by robert.murphy ▴ 80
0
votes
1
reply
1.5k
views
Comment: C: Can I use deseq on non transcriptome data?
4.3 years ago by robert.murphy ▴ 80
1
vote
11
replies
1.5k
views
Can I use deseq on non transcriptome data?
genome
4.3 years ago by robert.murphy ▴ 80
0
votes
1
reply
912
views
Comment: C: Cross referencing biosynthetic gene clusters in metagenome, best way to do this?
4.3 years ago by robert.murphy ▴ 80
0
votes
1
reply
15k
views
Comment: C: Deseq error : ncol(countData) == nrow(colData) is not TRUE
4.3 years ago by robert.murphy ▴ 80
4
votes
4
replies
912
views
Cross referencing biosynthetic gene clusters in metagenome, best way to do this?
genome
updated 4.3 years ago by ★ 27k • written 4.3 years ago by ▴ 80
0
votes
0
replies
1.5k
views
Comment: C: Can I use deseq on non transcriptome data?
4.3 years ago by robert.murphy ▴ 80
0
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0
replies
1.5k
views
Comment: C: Can I use deseq on non transcriptome data?
4.3 years ago by robert.murphy ▴ 80
0
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2
replies
1.0k
views
Comment: C: Blastn on paired end barcoding sequences
4.3 years ago by robert.murphy ▴ 80
0
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1
reply
1.0k
views
Comment: C: Blastn on paired end barcoding sequences
4.3 years ago by robert.murphy ▴ 80
0
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0
replies
1.0k
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Comment: C: Blastn on paired end barcoding sequences
4.3 years ago by robert.murphy ▴ 80
0
votes
13
replies
1.0k
views
Blastn on paired end barcoding sequences
sequencing genome
4.3 years ago by robert.murphy ▴ 80
0
votes
1
reply
1.0k
views
Comment: C: Blastn on paired end barcoding sequences
4.3 years ago by robert.murphy ▴ 80
0
votes
1
reply
1.0k
views
Comment: C: Blastn on paired end barcoding sequences
4.3 years ago by robert.murphy ▴ 80
0
votes
1
reply
934
views
Comment: C: Question: Best approach to bacterial hybrid genome assembly
4.4 years ago by robert.murphy ▴ 80
2
votes
3
replies
934
views
Question: Best approach to bacterial hybrid genome assembly
Assembly genome hybrid assembly
4.4 years ago by robert.murphy ▴ 80
0
votes
1
reply
7.4k
views
Comment: C: What is the difference between paired end reads and overlapping reads, and then
4.5 years ago by robert.murphy ▴ 80
0
votes
1
reply
7.4k
views
Comment: C: What is the difference between paired end reads and overlapping reads, and then
4.5 years ago by robert.murphy ▴ 80
8
votes
8
replies
7.4k
views
What is the difference between paired end reads and overlapping reads, and then why merge overlapping reads before assembly?
Assembly genome sequencing
updated 2.3 years ago by 15k • written 4.5 years ago by ▴ 80
181 results • Page 4 of 4
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