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1
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2.4k
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Estimating PSMC -p parameter and missing heterozygotes
PSMC
updated 4.4 years ago by 20 • written 9.1 years ago by ▴ 380
0
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0
replies
5.0k
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Comment: C: Tree input for PAML ancestral state reconstruction
updated 5.4 years ago by 45k • written 9.4 years ago by ▴ 380
0
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1
reply
3.0k
views
Comment: C: makeblastdb and blast very slow for 1 Ensembl genome, not for others
updated 5.5 years ago by 45k • written 9.6 years ago by ▴ 380
0
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0
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5.3k
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Comment: C: Method for generating a reference-based genome assembly in fasta with no referen
7.0 years ago by memory_donk ▴ 380
0
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5
replies
3.0k
views
makeblastdb and blast very slow for 1 Ensembl genome, not for others
blast genome
updated 8.1 years ago by • 0 • written 9.6 years ago by ▴ 380
0
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0
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2.7k
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Comment: C: Problem improving mammal contig assemblies
8.2 years ago by memory_donk ▴ 380
0
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0
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2.7k
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Comment: C: Problem improving mammal contig assemblies
8.2 years ago by memory_donk ▴ 380
0
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0
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2.5k
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Answer: A: Platanus file format error
8.2 years ago by memory_donk ▴ 380
0
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0
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2.4k
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Is baseml (PAML) suitable for ancestral reconstruction of non-coding sequences?
ancestral reconstruction evolution
8.2 years ago by memory_donk ▴ 380
0
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0
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2.9k
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Comment: C: Gene Ontology term enrichment tools that count duplicate/redundant genes
8.2 years ago by memory_donk ▴ 380
1
vote
2
replies
2.9k
views
Gene Ontology term enrichment tools that count duplicate/redundant genes
GeneOntology Ontology GO Genomics
updated 8.2 years ago by 9.0k • written 8.2 years ago by ▴ 380
0
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0
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2.7k
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Comment: C: Problem improving mammal contig assemblies
8.3 years ago by memory_donk ▴ 380
0
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0
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2.7k
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Comment: C: Problem improving mammal contig assemblies
8.3 years ago by memory_donk ▴ 380
6
votes
10
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2.7k
views
Problem improving mammal contig assemblies
Assembly genome
updated 8.3 years ago by 35k • written 8.3 years ago by ▴ 380
0
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0
replies
2.7k
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Comment: C: Problem improving mammal contig assemblies
8.3 years ago by memory_donk ▴ 380
1
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1
reply
2.7k
views
Comment: C: Problem improving mammal contig assemblies
8.3 years ago by memory_donk ▴ 380
0
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0
replies
1.5k
views
Scripting method to parse fastq diploid consensus sequence bins based on quality
fastq parsing bioperl biopython
9.1 years ago by memory_donk ▴ 380
6
votes
1
reply
6.4k
views
How to calculate p-value from codeml likelihood ratio test results for Benjamini-Hochberg correction
statistics PAML codeml LRT
9.1 years ago by memory_donk ▴ 380
5
votes
0
replies
6.4k
views
Answer: A: How to calculate p-value from codeml likelihood ratio test results for Benjamini
9.1 years ago by memory_donk ▴ 380
4
votes
1
reply
3.6k
views
Answer: A: How To Get Ensembl Id (Gene, Transcript, Protein) Information?
9.2 years ago by memory_donk ▴ 380
0
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0
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2.1k
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Comment: C: perl scriot for fasta
9.3 years ago by memory_donk ▴ 380
21
votes
0
replies
10k
views
Answer: Answer: Why does base quality of reads generally decreases at the end of the read?
updated 2.8 years ago by 45k • written 9.3 years ago by ▴ 380
0
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0
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1.8k
views
Answer: Answer: How to fix mates in PE Illumina data after alignment and discard reads with no m
updated 3.1 years ago by 45k • written 9.3 years ago by ▴ 380
5
votes
3
replies
5.0k
views
Tree input for PAML ancestral state reconstruction
gene software-error
updated 2.8 years ago by 45k • written 9.4 years ago by ▴ 380
2
votes
3
replies
5.3k
views
Method for generating a reference-based genome assembly in fasta with no reference genome bases
SNP Assembly alignment
updated 2.8 years ago by 45k • written 9.6 years ago by ▴ 380
0
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0
replies
5.0k
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Comment: C: Single end or paired end for variant calling
9.6 years ago by memory_donk ▴ 380
0
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0
replies
5.0k
views
Comment: Comment: Single end or paired end for variant calling
updated 2.7 years ago by 45k • written 9.6 years ago by ▴ 380
0
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1
reply
5.0k
views
Comment: C: Single end or paired end for variant calling
9.6 years ago by memory_donk ▴ 380
0
votes
2
replies
5.0k
views
Comment: Comment: Single end or paired end for variant calling
updated 2.7 years ago by 45k • written 9.6 years ago by ▴ 380
4
votes
9
replies
5.0k
views
Single end or paired end for variant calling
SNP genome alignment
updated 2.7 years ago by 45k • written 9.6 years ago by ▴ 380
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