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C: how to get a readable scale on a particular R plot
3.7 years ago by
vmicrobio
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1.2k
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C: count number of references with at least one hit
4.3 years ago by
vmicrobio
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1.2k
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C: count number of references with at least one hit
4.3 years ago by
vmicrobio
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1.2k
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Comment:
C: count number of references with at least one hit
4.3 years ago by
vmicrobio
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2.8k
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Comment:
C: differences between bwa-mem paired and single reads
4.7 years ago by
vmicrobio
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5.6k
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C: How can I make a .bed file from my fasta?
5.4 years ago by
vmicrobio
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C: idxstats non mapped reads
5.6 years ago by
vmicrobio
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C: Create a custom exome .genome for IGV
5.6 years ago by
vmicrobio
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C: conversion of GFF3 formate to BED format
5.8 years ago by
vmicrobio
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5.2k
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C: Read a fasta file | Java
6.0 years ago by
vmicrobio
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C: Reference Genome for mapping and VCF file for Realignment in Yak (Bos grunniens)
6.1 years ago by
vmicrobio
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C: Reference Genome for mapping and VCF file for Realignment in Yak (Bos grunniens)
6.1 years ago by
vmicrobio
▴ 290
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Comment:
C: Reference Genome for mapping and VCF file for Realignment in Yak (Bos grunniens)
6.1 years ago by
vmicrobio
▴ 290
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959
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Comment:
C: How to retrieve all pentamer from a sequence?
6.2 years ago by
vmicrobio
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C: Principal Component Analysis: How many most variant genes should I take?
6.4 years ago by
vmicrobio
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C: count of reads having multiple references
6.5 years ago by
vmicrobio
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1.3k
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Comment:
C: How to highlight multiple references mapped reads?
6.5 years ago by
vmicrobio
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1.3k
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Comment:
C: How to highlight multiple references mapped reads?
6.5 years ago by
vmicrobio
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Comment:
C: How to highlight multiple references mapped reads?
6.5 years ago by
vmicrobio
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C: Good pratice for clinical NGS data pipelines
6.5 years ago by
vmicrobio
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Comment:
C: REsequencing Genome Assembly and Functional Gene annotation workflow?
6.7 years ago by
vmicrobio
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1.9k
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Comment:
C: REsequencing Genome Assembly and Functional Gene annotation workflow?
6.7 years ago by
vmicrobio
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C: How to submit bacterial genomes to the database?
6.7 years ago by
vmicrobio
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2.9k
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Comment:
C: When should you de novo assemble a whole-genome, and when should you simply alig
6.7 years ago by
vmicrobio
▴ 290
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2.9k
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Comment:
C: When should you de novo assemble a whole-genome, and when should you simply alig
6.8 years ago by
vmicrobio
▴ 290
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5.8k
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Comment:
C: How to plot venn diagram from vcf-compare output ?
6.8 years ago by
vmicrobio
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2.3k
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Comment:
C: Alignment of mutli-contig fasta files
6.8 years ago by
vmicrobio
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1.2k
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Comment:
C: species abundacy calculation
6.9 years ago by
vmicrobio
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7.1k
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Comment:
C: Isolating reads from specific region from bam file
7.0 years ago by
vmicrobio
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3.5k
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Comment:
C: ion torrent read mapping and variant caller
7.0 years ago by
vmicrobio
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1.8k
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Comment:
C: MIRA assembly error
7.0 years ago by
vmicrobio
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3.5k
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Comment:
C: ion torrent read mapping and variant caller
7.0 years ago by
vmicrobio
▴ 290
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4.0k
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Comment:
C: Different alignments rates with bwa mem (0%) and bowtie2 (82%)
7.1 years ago by
vmicrobio
▴ 290
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1
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11k
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Comment:
C: BAM to BIGWIG
7.1 years ago by
vmicrobio
▴ 290
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1
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11k
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Comment:
C: BAM to BIGWIG
7.1 years ago by
vmicrobio
▴ 290
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1
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11k
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Comment:
C: BAM to BIGWIG
7.1 years ago by
vmicrobio
▴ 290
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1.3k
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Comment:
C: How can I experimentally validate LOH?
7.1 years ago by
vmicrobio
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1.7k
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Comment:
A: how to determine seed if sample share a seed <=value
7.1 years ago by
vmicrobio
▴ 290
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92k
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Comment:
C: merge large amount of fastq files into a single one
7.2 years ago by
vmicrobio
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8.4k
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Comment:
C: BAM to FASTQ
7.3 years ago by
vmicrobio
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4.9k
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Comment:
C: Mapping scaffolds to another reference genome
7.3 years ago by
vmicrobio
▴ 290
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9.5k
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Comment:
C: Beginner in Python needs assistance with counting 'A's in DNA sequences
7.3 years ago by
vmicrobio
▴ 290
1
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1
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3.0k
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Comment:
C: alignment containing sequences from position a to b
7.3 years ago by
vmicrobio
▴ 290
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