#include "gbseq.h"#include <fstream>Enumerations | |
| enum | inftype { dna, protein } |
Functions | |
| void | processOneFile (string &infile, bool show, gbseq *seq) |
| void | getInputFiles (const char nameFile[], vector< string > &files) |
| void | usage () |
| int | main (int argc, char *argv[]) |
| enum inftype |
| void getInputFiles | ( | const char | nameFile[], | |
| vector< string > & | files | |||
| ) |
| int main | ( | int | argc, | |
| char * | argv[] | |||
| ) |
References dna, feature::dumpGeneName(), Ref::dumpKey(), gbseq::dumpOrgmap(), feature::dumpSubseq(), getInputFiles(), gbseq::init(), inputFileType, feature::loadGeneName(), Ref::loadKey(), gbseq::loadOrgmap(), feature::loadSubseq(), processOneFile(), protein, feature::PRTOUT, gbdate::setup(), and usage.
| void processOneFile | ( | string & | infile, | |
| bool | show, | |||
| gbseq * | seq | |||
| ) |
| void usage | ( | ) |
given gmap summary format, this program converts it into combest archive format (*.car)
It can be used a pipe, or given specific file names.
this is a helper program to count distinct estids in the ESTId column of the combest result. So it is the actual number of ESTs mapped. This could be lower for deeply covered genome because of the coverage depth-dependent filtering.
given gmap summary format, this program converts it into combest archive format (*.car)
It can be used a pipe, or given specific file names.
this is a helper program to count distinct estids in the ESTId column of the combest result. So it is the actual number of ESTs mapped. This could be lower for deeply covered genome because of the coverage depth-dependent filtering.
1.5.6