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Update README.md
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tomas-fer authored Jun 20, 2018
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1: Processing raw reads (PhiX removal, adaptor removal, quality filtering, summary statistics)
2: Mapping reads to reference (using Bowtie2/BWA), create consensus sequence
3: Recognize sequences matching probes (generate PSLX files using BLAT)
4: Create alignments for all genes (+ correct reading frame)
4: Create alignments for all genes (+ optionally correct reading frame and/or select low heterozygosity loci)
5: Treat missing data, select best genes
6: Generate FastTree or RAxML gene trees + calculate/plot trees-alignment properties
7: Root gene trees with outgroup, combine gene trees into a single file
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