Align Sequence Reads to a Reference Genome via Seed-and-Vote
Calculate Percentages of Nucleotides in Reads
Map and quantify single-cell RNA-seq data generated by 10X Genomics
Determine Detection P Values for Each Gene in an RNA-seq Dataset
Generate Annotation Data Used for Calculating Detection P Values
Finding the Common Variants Among All Input VCF Files
Flatten Features in GTF or GFF Annotation Files
Obtain Chromosomal Coordiates of Each Exon Using NCBI Annotation
Generate Annotation for Promoter Regions of Genes
Calculate the Proportion of Mapped Reads or Fragments in SAM/BAM Files
Extract Quality Score Data in a Sequencing Read Dataset
Remove Sequencing Reads Mapped to Identical Locations
Re-Order Paired-End Reads to Place Reads
Generate Simulated Reads from a Set of Transcripts
Align Long Sequence Reads to a Reference Genome via Seed-and-Vote
Count Number of Bases Unique to Each Transcript