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资源简介：
Custom scripts employed for the analysis of the sequencing data.
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创建时间：
2022-11-16
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IM-TORNADO: a tool for comparison of 16S reads from paired-end libraries
Motivation: 16S rDNA hypervariable tag sequencing has become the de facto method for accessing microbial diversity. Illumina paired-end sequencing, which produces two separate reads for each DNA fragm
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tiny example read set
one human read, one phiX read, and one E. coli read, prepared along with the db build on this page: https://hackmd.io/@astrobiomike/GL-kraken2-human-db-setup
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Additional file 2: of Ribosome signatures aid bacterial translation initiation site identification
Tables S1–S18. Table S1. Variable importance in the S. Typhimurium monosome sample. Table S2. Variable importance in the S. Typhimurium polysome sample. Table S3. N-terminal support for S. Typhimurium
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Additional file 2 of Variance of allele balance calculated from low coverage sequencing data infers departure from a diploid state
Additional file 2 Tables S1 Summary results for 1,000 tests simulating different ploidies and different levels of coverage; Table S2 SRA information and values calculated for downsampled data of Bremi
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Supplementary Data S3: Custom scripts used in this analysis
Scripts used in the development of this manuscript. See Genome_Diagram_Maker/README.txt for usage instructions.
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