geecee |
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geecee calculates the fraction of G+C bases of the input nucleic acid sequence(s). It sums the number of G and C bases in the input sequence(s) and writes the result to file as the fraction (in the interval 0.0 to 1.0) of the length of the whole sequence.
% geecee tembl:L46634 Calculate fractional GC content of nucleic acid sequences Output file [l46634.geecee]: |
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Calculate fractional GC content of nucleic acid sequences Version: EMBOSS:6.4.0.0 Standard (Mandatory) qualifiers: [-sequence] seqall Nucleotide sequence(s) filename and optional format, or reference (input USA) [-outfile] outfile [*.geecee] Output file name Additional (Optional) qualifiers: (none) Advanced (Unprompted) qualifiers: (none) Associated qualifiers: "-sequence" associated qualifiers -sbegin1 integer Start of each sequence to be used -send1 integer End of each sequence to be used -sreverse1 boolean Reverse (if DNA) -sask1 boolean Ask for begin/end/reverse -snucleotide1 boolean Sequence is nucleotide -sprotein1 boolean Sequence is protein -slower1 boolean Make lower case -supper1 boolean Make upper case -sformat1 string Input sequence format -sdbname1 string Database name -sid1 string Entryname -ufo1 string UFO features -fformat1 string Features format -fopenfile1 string Features file name "-outfile" associated qualifiers -odirectory2 string Output directory General qualifiers: -auto boolean Turn off prompts -stdout boolean Write first file to standard output -filter boolean Read first file from standard input, write first file to standard output -options boolean Prompt for standard and additional values -debug boolean Write debug output to program.dbg -verbose boolean Report some/full command line options -help boolean Report command line options and exit. More information on associated and general qualifiers can be found with -help -verbose -warning boolean Report warnings -error boolean Report errors -fatal boolean Report fatal errors -die boolean Report dying program messages -version boolean Report version number and exit |
Qualifier | Type | Description | Allowed values | Default |
---|---|---|---|---|
Standard (Mandatory) qualifiers | ||||
[-sequence] (Parameter 1) |
seqall | Nucleotide sequence(s) filename and optional format, or reference (input USA) | Readable sequence(s) | Required |
[-outfile] (Parameter 2) |
outfile | Output file name | Output file | <*>.geecee |
Additional (Optional) qualifiers | ||||
(none) | ||||
Advanced (Unprompted) qualifiers | ||||
(none) | ||||
Associated qualifiers | ||||
"-sequence" associated seqall qualifiers | ||||
-sbegin1 -sbegin_sequence |
integer | Start of each sequence to be used | Any integer value | 0 |
-send1 -send_sequence |
integer | End of each sequence to be used | Any integer value | 0 |
-sreverse1 -sreverse_sequence |
boolean | Reverse (if DNA) | Boolean value Yes/No | N |
-sask1 -sask_sequence |
boolean | Ask for begin/end/reverse | Boolean value Yes/No | N |
-snucleotide1 -snucleotide_sequence |
boolean | Sequence is nucleotide | Boolean value Yes/No | N |
-sprotein1 -sprotein_sequence |
boolean | Sequence is protein | Boolean value Yes/No | N |
-slower1 -slower_sequence |
boolean | Make lower case | Boolean value Yes/No | N |
-supper1 -supper_sequence |
boolean | Make upper case | Boolean value Yes/No | N |
-sformat1 -sformat_sequence |
string | Input sequence format | Any string | |
-sdbname1 -sdbname_sequence |
string | Database name | Any string | |
-sid1 -sid_sequence |
string | Entryname | Any string | |
-ufo1 -ufo_sequence |
string | UFO features | Any string | |
-fformat1 -fformat_sequence |
string | Features format | Any string | |
-fopenfile1 -fopenfile_sequence |
string | Features file name | Any string | |
"-outfile" associated outfile qualifiers | ||||
-odirectory2 -odirectory_outfile |
string | Output directory | Any string | |
General qualifiers | ||||
-auto | boolean | Turn off prompts | Boolean value Yes/No | N |
-stdout | boolean | Write first file to standard output | Boolean value Yes/No | N |
-filter | boolean | Read first file from standard input, write first file to standard output | Boolean value Yes/No | N |
-options | boolean | Prompt for standard and additional values | Boolean value Yes/No | N |
-debug | boolean | Write debug output to program.dbg | Boolean value Yes/No | N |
-verbose | boolean | Report some/full command line options | Boolean value Yes/No | Y |
-help | boolean | Report command line options and exit. More information on associated and general qualifiers can be found with -help -verbose | Boolean value Yes/No | N |
-warning | boolean | Report warnings | Boolean value Yes/No | Y |
-error | boolean | Report errors | Boolean value Yes/No | Y |
-fatal | boolean | Report fatal errors | Boolean value Yes/No | Y |
-die | boolean | Report dying program messages | Boolean value Yes/No | Y |
-version | boolean | Report version number and exit | Boolean value Yes/No | N |
The input is a standard EMBOSS sequence query (also known as a 'USA').
Major sequence database sources defined as standard in EMBOSS installations include srs:embl, srs:uniprot and ensembl
Data can also be read from sequence output in any supported format written by an EMBOSS or third-party application.
The input format can be specified by using the command-line qualifier -sformat xxx, where 'xxx' is replaced by the name of the required format. The available format names are: gff (gff3), gff2, embl (em), genbank (gb, refseq), ddbj, refseqp, pir (nbrf), swissprot (swiss, sw), dasgff and debug.
See: http://emboss.sf.net/docs/themes/SequenceFormats.html for further information on sequence formats.
ID L46634; SV 1; linear; genomic DNA; STD; VRL; 1272 BP. XX AC L46634; L46689; XX DT 06-NOV-1995 (Rel. 45, Created) DT 04-MAR-2000 (Rel. 63, Last updated, Version 3) XX DE Human herpesvirus 7 (clone ED132'1.2) telomeric repeat region. XX KW telomeric repeat. XX OS Human herpesvirus 7 OC Viruses; dsDNA viruses, no RNA stage; Herpesvirales; Herpesviridae; OC Betaherpesvirinae; Roseolovirus. XX RN [1] RP 1-1272 RX PUBMED; 7494318. RA Secchiero P., Nicholas J., Deng H., Xiaopeng T., van Loon N., Ruvolo V.R., RA Berneman Z.N., Reitz M.S.Jr., Dewhurst S.; RT "Identification of human telomeric repeat motifs at the genome termini of RT human herpesvirus 7: structural analysis and heterogeneity"; RL J. Virol. 69(12):8041-8045(1995). XX FH Key Location/Qualifiers FH FT source 1..1272 FT /organism="Human herpesvirus 7" FT /strain="JI" FT /mol_type="genomic DNA" FT /clone="ED132'1.2" FT /db_xref="taxon:10372" FT repeat_region 207..928 FT /note="long and complex repeat region composed of various FT direct repeats, including TAACCC (TRS), degenerate copies FT of TRS motifs and a 14-bp repeat, TAGGGCTGCGGCCC" FT misc_signal 938..998 FT /note="pac2 motif" FT misc_feature 1009 FT /note="right genome terminus (...ACA)" XX SQ Sequence 1272 BP; 346 A; 455 C; 222 G; 249 T; 0 other; aagcttaaac tgaggtcaca cacgacttta attacggcaa cgcaacagct gtaagctgca 60 ggaaagatac gatcgtaagc aaatgtagtc ctacaatcaa gcgaggttgt agacgttacc 120 tacaatgaac tacacctcta agcataacct gtcgggcaca gtgagacacg cagccgtaaa 180 ttcaaaactc aacccaaacc gaagtctaag tctcacccta atcgtaacag taaccctaca 240 actctaatcc tagtccgtaa ccgtaacccc aatcctagcc cttagcccta accctagccc 300 taaccctagc tctaacctta gctctaactc tgaccctagg cctaacccta agcctaaccc 360 taaccgtagc tctaagttta accctaaccc taaccctaac catgaccctg accctaaccc 420 tagggctgcg gccctaaccc tagccctaac cctaacccta atcctaatcc tagccctaac 480 cctagggctg cggccctaac cctagcccta accctaaccc taaccctagg gctgcggccc 540 taaccctaac cctagggctg cggcccgaac cctaacccta accctaaccc taaccctagg 600 gctgcggccc taaccctaac cctagggctg cggccctaac cctaacccta gggctgcggc 660 ccgaacccta accctaaccc taaccctagg gctgcggccc taaccctaac cctagggctg 720 cggccctaac cctaacccta actctagggc tgcggcccta accctaaccc taaccctaac 780 cctagggctg cggcccgaac cctagcccta accctaaccc tgaccctgac cctaacccta 840 accctaaccc taaccctaac cctaacccta accctaaccc taaccctaac cctaacccta 900 accctaaccc taaccctaac cctaaccccg cccccactgg cagccaatgt cttgtaatgc 960 cttcaaggca ctttttctgc gagccgcgcg cagcactcag tgaaaaacaa gtttgtgcac 1020 gagaaagacg ctgccaaacc gcagctgcag catgaaggct gagtgcacaa ttttggcttt 1080 agtcccataa aggcgcggct tcccgtagag tagaaaaccg cagcgcggcg cacagagcga 1140 aggcagcggc tttcagactg tttgccaagc gcagtctgca tcttaccaat gatgatcgca 1200 agcaagaaaa atgttctttc ttagcatatg cgtggttaat cctgttgtgg tcatcactaa 1260 gttttcaagc tt 1272 // |
#Sequence GC content L46634 0.53 |
The first non-blank line is the title line. Subsequent lines consist of two columns of data.
Program name | Description |
---|---|
cpgplot | Identify and plot CpG islands in nucleotide sequence(s) |
cpgreport | Identify and report CpG-rich regions in nucleotide sequence(s) |
newcpgreport | Identify CpG islands in nucleotide sequence(s) |
newcpgseek | Identify and report CpG-rich regions in nucleotide sequence(s) |
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