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hbctraining
/
variant_analysis
https://hbctraining.github.io/variant_analysis/
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PoN
#16
Gammerdinger
opened
2 months ago
1
Intro lecture: DNA quantity/handling considerations for long read sequencing
#15
epartan
opened
2 months ago
0
Answers and explanations for exercises of intro lesson 00
#14
naurasd
opened
4 months ago
2
-cancerSamples
#13
Gammerdinger
opened
6 months ago
0
maybe a tree command check before AlignmentQC
#12
mistrm82
opened
6 months ago
0
add a multiqc run after snpeff?
#11
mistrm82
opened
6 months ago
0
"Next Lesson" link from 00 intro does not work, links to main page instead
#10
epartan
closed
6 months ago
1
self-learning.md links
#9
benjibromberg
closed
7 months ago
2
Command executed:GRCh38.p14
#8
singha30
closed
2 months ago
1
hg38.fa.genome
#7
singha30
closed
11 months ago
2
changes to 03_fastqc.md
#6
mistrm82
closed
6 months ago
0
changes to 02_project_organization.md
#5
mistrm82
closed
6 months ago
1
add content to syn dataset lesson
#4
mistrm82
closed
6 months ago
1
create an intro to variant calling md
#3
mistrm82
closed
6 months ago
4
Mmedits fastqc trim
#2
rkhetani
closed
1 year ago
0
First Variant Call Format draft
#1
Gammerdinger
closed
2 years ago
0