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This Programm verifies which 16S variable region was sequenced.

Input: .fastq file containing 16S sequencing reads or a Directory containing (or subfolders containing) fasta or fastq files Output: print(Probabilities for every region) CSV file containing read_designation, Percentage unaligned reads, Probabilities of every region

Requirements: python 3 bowtie2 samtools bedtools

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predict variable region from amplicon sequences

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