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phenomut

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To identify the mutation that causes change in phenotype for C. elegans, we have developed two PERL scripts (Step A and Step C). Pre-requisite: Pre-installed BFAST, SAMTOOLS, and ANNOVAR software programs and the paths Input: Fastq file(s) for F2s that is homozygous for the mutation. USAGE: Step A: Alignment, SNP calling, annotation, adding SNP count, and selecting homozygous mutants (based on MutFinder_v_0.1.0.pl) Download PhenoMut_Step_A_v_0.1.0.pl and postprocessing_v2.pl Type "perl PhenoMut_Step_A_v_0.1.0.pl" (Answer questions) Type "source PhenoMut_Step_A_v_0.1.0.sh" Step B: Manually finding the interval of interest Draw Hawaiian SNP percentage (Y-axis) as a function of chromosome position (X-axis) for each chromosome using Microsoft Excel or other software (hawaiian_SNP_I.txt, hawaiian_SNP_II.txt, etc.) De

文 件 列 表

extracting_hawaiian_SNPs_v_0.1.0.pl
PhenoMut_Step_A_v_0.1.0.pl
PhenoMut_Step_C_v_0.1.0.pl
Hawaiian_SNPs.txt

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