quast.sh | assembly stats | Uses QUAST to assess quality of genome assemblies | Genome before filtering/softmasking & Genome after filtering/softmasking | Assembly statistics for both inputs |
quast.sh | assembly stats | Uses QUAST to assess quality of genome assemblies | Genome before filtering/softmasking & Genome after filtering/softmasking | Assembly statistics for both inputs |
#### Preparing TSA
#### Preparing TSA Files
Processing the TSA files from NCBI to be used as evidence for genome annotation tool was accomplished by frame-selecting using [TransDecoder](https://github.com/TransDecoder/TransDecoder/wiki) and clustering with [USearch (v9.0)](https://www.drive5.com/usearch/manual9/).
Processing the TSA files from NCBI to be used as evidence for genome annotation tool was accomplished by frame-selecting using [TransDecoder](https://github.com/TransDecoder/TransDecoder/wiki) and clustering with [USearch (v9.0)](https://www.drive5.com/usearch/manual9/).
Short-read and TSA evidence were aligned to genome assemblies using [HISAT2](https://ccb.jhu.edu/software/hisat2/manual.shtml) and [GMAP](http://research-pub.gene.com/gmap/src/README), respectively. Before alignment, short-reads evidence was trimmed QC'd using sickle and [FastQC](https://www.bioinformatics.babraham.ac.uk/projects/fastqc/).
Short-read and TSA evidence were aligned to genome assemblies using [HISAT2](https://ccb.jhu.edu/software/hisat2/manual.shtml) and [GMAP](http://research-pub.gene.com/gmap/src/README), respectively. Before alignment, short-reads evidence was trimmed QC'd using sickle and [FastQC](https://www.bioinformatics.babraham.ac.uk/projects/fastqc/).