ANGSD: Analysis of next generation Sequencing Data

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Genotype Likelihoods: Difference between revisions

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; -GL [int]
; -GL [int]
If your input is sequencing file you can estimate genotype likelhoods from the mapped reads. Four different methods are available.  
If your input is sequencing file you can estimate genotype likelhoods from the mapped reads. Four different methods are available.  
===soapSNP===
-GL 0
===Samtools===
===Samtools===
-GL 1
-GL 1
===GATK===
===GATK===
-GL 2
-GL 2
===soapSNP===
-GL 3
===Kim et al.===
===Kim et al.===
-GL 3
-GL 4
[[Kim10|Citation]] [[Kim11|Citation]]
[[Kim10|Citation]] [[Kim11|Citation]]

Revision as of 20:47, 18 June 2012

Genotype likelihoods from alignments

-GL [int]

If your input is sequencing file you can estimate genotype likelhoods from the mapped reads. Four different methods are available.

Samtools

-GL 1

GATK

-GL 2

soapSNP

-GL 3

Kim et al.

-GL 4 Citation Citation