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README.md

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# Clair3-RNA
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# Clair3-RNA - long-read short variant caller for RNA sequencing data
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[![License](https://img.shields.io/badge/License-BSD%203--Clause-blue.svg)](https://opensource.org/licenses/BSD-3-Clause)
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Minimum Indel AF required for a candidate variant to be called. Default: ont:0.15,hifi:0.08.
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--min_coverage MIN_COVERAGE
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Minimal coverage required for a variant to be called. Default: 4.
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--tag_variant_using_readiportal
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Tag variants uisng REDIportal dataset, If set, called variants that are also in the readiportal dataset will be marked as "RNAEditing". Default: disable.
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--readiportal_database_filter_tag READIPORTAL_DATABASE_FILTER_TAG
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Use only editing sites with these tags in the readiportal dataset, split by ":" for multiple tags. Default: using sites supported by two or more sources - "A,D:A,R:A,R,D".
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--readiportal_reference_genome_version READIPORTAL_REFERENCE_GENOME_VERSION
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Select the reference genome version in the readiportal dataset. Possible options: {grch38, grch37}. Default: "grch38".
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--chunk_size CHUNK_SIZE
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The size of each chuck for parallel processing. Default: 5000000.
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-s SAMPLE_NAME, --sample_name SAMPLE_NAME
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--samtools SAMTOOLS Absolute path of samtools, samtools version >= 1.10 is required.
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--parallel PARALLEL Absolute path of parallel, parallel >= 20191122 is required.
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--min_mq MIN_MQ Minimal mapping quality required for an alignment to be considered. Default: 5.
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--tag_variant_using_readiportal
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Tag variants uisng REDIportal dataset, If set, variants in the readiportal dataset will be marked as "RNAEditing". Default: disable.
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--readiportal_database_filter_tag READIPORTAL_DATABASE_FILTER_TAG
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Use only editing sites with these tags in the readiportal dataset, split by ":" for multiple tags. Default: using sites supported by two or more sources - "A,D:A,R:A,R,D".
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--readiportal_reference_genome_version READIPORTAL_REFERENCE_GENOME_VERSION
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Select the reference genome version in the readiportal dataset. Possible options: {grch38, grch37}. Default: "grch38".
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```
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#### Call variants in one or mutiple chromosomes using the `-C/--ctg_name` parameter

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