added Bai et al. Seems good, too.
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@ -156,14 +156,16 @@ have ignored these important genes.
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We recommend to include the genomic regions of classical HLA genes in the BWA
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index. This way we will be able to get a more complete collection of reads
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mapped to HLA. We can then isolate these reads with little computational cost
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and type HLA genes with another program, such as [Liu et al (2013)][hla2],
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[Dilthey et al (2014)][hla1] or one from [this list][hlatools].
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and type HLA genes with another program, such as [Liu et al (2013)][hla2], [Bai
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et al (2014)][hla3], [Dilthey et al (2014)][hla1] or one from [this
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list][hlatools].
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If the postprocessing script `bwa-postalt.js` is invoked with `-p prefix`, it
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will also write the top three alleles to file `prefix.hla`. However, as most HLA
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alleles from IMGT/HLA don't have intronic sequences and thus are not included in
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the reference genome, we are unable to type HLA genes to high resolution with
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the BWA-MEM mapping alone. A dedicated tool is recommended for accurate typing.
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the BWA index from option 2, we are unable to type HLA genes to high resolution
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with the BWA-MEM mapping alone. A dedicated tool is recommended for accurate
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typing.
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### Evaluating ALT Mapping
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@ -195,3 +197,4 @@ can even get rid of ALT contigs for good.
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[hlalink]: http://www.hladiseaseassociations.com
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[hlatools]: https://www.biostars.org/p/93245/
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[hla2]: http://nar.oxfordjournals.org/content/41/14/e142.full.pdf+html
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[hla3]: http://www.biomedcentral.com/1471-2164/15/325
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