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16
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Forum: What do you work on while waiting on your programs to finish?
fun
updated 12 months ago by 43k • written 7.6 years ago by ▴ 740
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Comment: C: EDIT: Repeat region drop out
7.6 years ago by skbrimer ▴ 740
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1.4k
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Comment: C: EDIT: Repeat region drop out
7.6 years ago by skbrimer ▴ 740
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1.4k
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EDIT: Repeat region drop out
Assembly
7.7 years ago by skbrimer ▴ 740
14
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4
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27k
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Samtools 1.3 bam to fastq
software error
updated 7.7 years ago by 20 • written 8.1 years ago by ▴ 740
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Comment: C: Determining inhouse cut offs
7.7 years ago by skbrimer ▴ 740
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Comment: C: Determining inhouse cut offs
7.7 years ago by skbrimer ▴ 740
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1.5k
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Comment: C: Determining inhouse cut offs
7.7 years ago by skbrimer ▴ 740
4
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6
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1.5k
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Determining inhouse cut offs
coverage
updated 12 months ago by 43k • written 7.7 years ago by ▴ 740
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0
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1.5k
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Comment: C: Interpreting de novo contig output
7.8 years ago by skbrimer ▴ 740
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1.5k
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Comment: C: Interpreting de novo contig output
7.8 years ago by skbrimer ▴ 740
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1.5k
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Comment: C: Interpreting de novo contig output
7.8 years ago by skbrimer ▴ 740
1
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6
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1.5k
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Interpreting de novo contig output
de novo RNA-Seq
7.8 years ago by skbrimer ▴ 740
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1
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2.1k
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Comment: C: IGV-results of Bowtie mapping, strange colors!
7.9 years ago by skbrimer ▴ 740
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2.1k
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Answer: A: IGV-results of Bowtie mapping, strange colors!
7.9 years ago by skbrimer ▴ 740
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7.6k
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Comment: C: Controls for Sequencing
7.9 years ago by skbrimer ▴ 740
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7.6k
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Comment: C: Controls for Sequencing
7.9 years ago by skbrimer ▴ 740
1
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7.6k
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Comment: C: Controls for Sequencing
7.9 years ago by skbrimer ▴ 740
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Answer: A: VICUNA - how to select optional reference guided merging of contigs
8.0 years ago by skbrimer ▴ 740
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0
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4.2k
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Comment: C: calculating within population nucleotide diversity for a virus population
8.1 years ago by skbrimer ▴ 740
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27k
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Comment: C: Samtools 1.3 bam to fastq
8.1 years ago by skbrimer ▴ 740
0
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1
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27k
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Comment: C: Samtools 1.3 bam to fastq
8.1 years ago by skbrimer ▴ 740
11
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1
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27k
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Answer: A: Samtools 1.3 bam to fastq
8.1 years ago by skbrimer ▴ 740
1
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1
reply
11k
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Answer: A: Why GATK and bcftools SNP calling different?
8.1 years ago by skbrimer ▴ 740
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1
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11k
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Comment: C: Why GATK and bcftools SNP calling different?
8.1 years ago by skbrimer ▴ 740
2
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Answer: A: ***EDIT*** BioPython: how to edit a fasta file to include a large deletion
8.1 years ago by skbrimer ▴ 740
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Comment: C: ***EDIT*** BioPython: how to edit a fasta file to include a large deletion
8.1 years ago by skbrimer ▴ 740
1
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Answer: A: EDIT:SOLVED:changing the fasta header in a multi-fasta file with biopython.
8.1 years ago by skbrimer ▴ 740
2
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3
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5.3k
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EDIT:SOLVED:changing the fasta header in a multi-fasta file with biopython.
biopython
8.1 years ago by skbrimer ▴ 740
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1
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4.6k
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Comment: C: ***EDIT*** BioPython: how to edit a fasta file to include a large deletion
8.1 years ago by skbrimer ▴ 740
15
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25
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2.5k
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6 follow
Forum: How to get help on a question that has been buried?
meta biostars
updated 14 months ago by 43k • written 8.1 years ago by ▴ 740
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1
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8.2k
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Comment: C: Filtering of low coverage variants from VCF
8.1 years ago by skbrimer ▴ 740
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4.6k
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Comment: C: ***EDIT*** Need help with a python script to: Annotation of a large drop out in
8.1 years ago by skbrimer ▴ 740
1
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0
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2.4k
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Answer: A: Get location based on protein ids from genbankfile
8.1 years ago by skbrimer ▴ 740
1
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1
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8.2k
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Answer: A: Filtering of low coverage variants from VCF
8.1 years ago by skbrimer ▴ 740
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0
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2.5k
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Comment: C: How to get help on a question that has been buried?
8.1 years ago by skbrimer ▴ 740
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0
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2.5k
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Comment: C: How to get help on a question that has been buried?
8.1 years ago by skbrimer ▴ 740
0
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1
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2.5k
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Comment: C: How to get help on a question that has been buried?
8.1 years ago by skbrimer ▴ 740
0
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0
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5.3k
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Comment: C: changing the fasta header in a multi-fasta file with biopython.
8.1 years ago by skbrimer ▴ 740
0
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0
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2.0k
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Answer: A: Detecting structural variants when comparing assembled genome and reference
8.1 years ago by skbrimer ▴ 740
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0
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4.6k
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Comment: C: Annotation of a large drop out in a bacterial genome
8.2 years ago by skbrimer ▴ 740
0
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0
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4.3k
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Answer: A: Help constructing a restriction map of a linear fragment of DNA?
8.2 years ago by skbrimer ▴ 740
3
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3
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6.0k
views
Bed file loading issues
igv Bed
updated 21 months ago by 43k • written 8.3 years ago by ▴ 740
3
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3
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2.1k
views
More file parsing :) ***EDIT*** how do I make a fast and bed file from Genbank file - SOLVED
biopython
updated 21 months ago by 43k • written 8.3 years ago by ▴ 740
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0
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2.1k
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Comment: C: More file parsing :)
8.3 years ago by skbrimer ▴ 740
2
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0
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4.1k
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Answer: Answer: Biopython script to change file formats and headers
updated 3.1 years ago by 43k • written 8.3 years ago by ▴ 740
3
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4
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4.1k
views
Biopython script to change file formats and headers
biopython processing
updated 3.1 years ago by 43k • written 8.3 years ago by ▴ 740
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1
reply
2.4k
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Answer: Answer: Tools For Analyzing Copy Number Variation
updated 21 months ago by 43k • written 8.4 years ago by ▴ 740
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0
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2.7k
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Comment: C: Building a pipeline
8.5 years ago by skbrimer ▴ 740
5
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6
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2.7k
views
Building a pipeline
RNA-Seq analysis ngs snakemake reporting
updated 2.6 years ago by 43k • written 8.5 years ago by ▴ 740
190 results • Page 3 of 4
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