Platform: Illumina NovaSeq dandamali, PE150
Nau'in ɗakin karatu: 350bp saka ɗakin karatu na cDNA (ya danganta da mafi girman rarraba)
Dabarar jeri: Haɗa-Ƙarshen 150 bp
Adadin bayanai: 2 Gb raw data/samfuri
(1) Sequencing data ingancin iko: Nucleotide rarraba, Tushen ingancin rarraba, rRNA rabo kima;
(2) Binciken jeri-jeri: Ƙididdiga sakamakon daidaitawa, Cikewa na jeri, Rufe jerin;
(3) Bayanin bayanan kwayoyin halitta (NR, Swiss-Prot, Pfam, COG, GO, KEGG);
(4) Binciken Magana: Rarraba magana (Tare da samfurori guda biyu ko fiye), Nazarin magana tsakanin samfurori (bincike na Venn, Binciken Daidaitawa, PCA bincike);
(5) Binciken maganganu daban-daban (Tare da samfurori biyu ko fiye);
(6) Binciken saiti na Gene: Binciken Venn, Binciken Cluster, Nazarin bayanin aiki (COG, GO, KEGG), Binciken haɓaka aikin aiki (GO, KEGG), jadawali haɓaka aikin haɓakawa, nazarin Ipath;
(7) sRNA bincike: sRNA tsinkaya, sRNA annotation (Blast, sRNAMap, sRNATarBase, SIPHT, Rfam), sRNA tsarin sakandare tsinkaya, sRNA manufa tsinkaya;
(8) Binciken tsarin kwafi: Binciken Operon, Rubutu farawa da ƙarshen hasashen shafukan yanar gizo, UTR annotation da bincike, Hasashen jerin abubuwan haɓakawa, SNP/InDel bincike (SNP/InDel annotation, SNP/InDel rarraba yanki, SNP statistics).