We are interested in incorporating bulk RNAseq Emory Vascular dataset (Emory_Vascular - syn18909507) in our analyses, and we would like to know if there are files available describing the quality control process for generating the processed RNAseq data. We are interested in the following: 1 - Fastqc files or information on per base sequence quality, per base sequence content, insert size ( if paired end ). 2 - Information on how read counts files were generated from fastq. fastq - > bam: which aligner is used, any intermediate files listing alignment stats. bam -> read counts: which quantification tool and gene annotation files were used. Thank you, Samantha