Hi I am working on wheat RNA seq Data obtained via High Throughput Sequencing , as i am new to this work i am confused for input file required for DAVID > https://david-d.ncifcrf.gov/conversion.jsp?VFROM=NA. The nature protocol states about input file as:-
A list of gene identifiers is the only required input for all DAVID analytic modules or tools. The gene list may be derived from any type of high- throughput genomic, computational or proteomic study, such as DNA expression microarray, proteomics, CHIP-on-CHIP, SNP array, CHIP-sequence and so on.
It would be really helpful if someone has a Solution on How to produce input (list of gene identifiers) files for this tool.
Thanking in Advacne
Align the data to the reference genome and then qualify transcripts and you can use the transcript list as an input list for DAVID analysis.
List of gene is a simple list. See this help page. You will need to ensure that the identifiers used work with DAVID.