QUAST report
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Contigs are ordered from largest (contig #1) to smallest. Contigs are broken into nonoverlapping 100 bp windows. Plot shows numbers of windows for each GC percentage. |
{"date":"28 December 2014, Sunday, 23:01:37","report":[["Statistics without reference",[{"values":[1,1,1,1,1],"quality":"Less is better","isMain":true,"metricName":"# contigs"},{"values":[1,1,1,1,1],"quality":"Less is better","isMain":false,"metricName":"# contigs (>= 0 bp)"},{"values":[1,1,1,1,1],"quality":"Less is better","isMain":false,"metricName":"# contigs (>= 1000 bp)"},{"values":[4644061,4651184,4644056,4651207,4651348],"quality":"More is better","isMain":true,"metricName":"Largest contig"},{"values":[4644061,4651184,4644056,4651207,4651348],"quality":"More is better","isMain":true,"metricName":"Total length"},{"values":[4644061,4651184,4644056,4651207,4651348],"quality":"More is better","isMain":false,"metricName":"Total length (>= 0 bp)"},{"values":[4644061,4651184,4644056,4651207,4651348],"quality":"More is better","isMain":false,"metricName":"Total length (>= 1000 bp)"},{"values":[4644061,4651184,4644056,4651207,4651348],"quality":"More is better","isMain":true,"metricName":"N50"},{"values":[4644061,4651184,4644056,4651207,4651348],"quality":"More is better","isMain":false,"metricName":"N75"},{"values":[1,1,1,1,1],"quality":"Less is better","isMain":false,"metricName":"L50"},{"values":[1,1,1,1,1],"quality":"Less is better","isMain":false,"metricName":"L75"},{"values":["50.78","50.78","50.78","50.78","50.78"],"quality":"Equal","isMain":false,"metricName":"GC (%)"}]],["Misassemblies",[{"values":[8,8,8,8,8],"quality":"Less is better","isMain":true,"metricName":"# misassemblies"},{"values":[7,7,7,7,7],"quality":"Less is better","isMain":false,"metricName":" # relocations"},{"values":[0,0,0,0,0],"quality":"Less is better","isMain":false,"metricName":" # translocations"},{"values":[1,1,1,1,1],"quality":"Less is better","isMain":false,"metricName":" # inversions"},{"values":[1,1,1,1,1],"quality":"Less is better","isMain":false,"metricName":"# misassembled contigs"},{"values":[4644061,4651184,4644056,4651207,4651348],"quality":"Less is better","isMain":true,"metricName":"Misassembled contigs length"},{"values":[3,4,3,4,3],"quality":"Less is better","isMain":false,"metricName":"# local misassemblies"}]],["Unaligned",[{"values":[0,0,0,0,0],"quality":"Less is better","isMain":false,"metricName":"# fully unaligned contigs"},{"values":[0,0,0,0,0],"quality":"Less is better","isMain":false,"metricName":"Fully unaligned length"},{"values":[0,0,0,0,0],"quality":"Less is better","isMain":false,"metricName":"# partially unaligned contigs"},{"values":[0,0,0,0,0],"quality":"Less is better","isMain":false,"metricName":" # with misassembly"},{"values":[0,0,0,0,0],"quality":"Less is better","isMain":false,"metricName":" # both parts are significant"},{"values":[0,0,0,0,0],"quality":"Less is better","isMain":false,"metricName":"Partially unaligned length"}]],["Mismatches",[{"values":[6,18,6,16,9],"quality":"Less is better","isMain":false,"metricName":"# mismatches"},{"values":[1454,1468,1451,1533,1421],"quality":"Less is better","isMain":false,"metricName":"# indels"},{"values":[1515,1606,1518,1691,1516],"quality":"Less is better","isMain":false,"metricName":"Indels length"},{"values":["0.13","0.39","0.13","0.34","0.19"],"quality":"Less is better","isMain":true,"metricName":"# mismatches per 100 kbp"},{"values":["31.34","31.64","31.27","33.04","30.63"],"quality":"Less is better","isMain":true,"metricName":"# indels per 100 kbp"},{"values":[1450,1457,1448,1523,1413],"quality":"Less is better","isMain":false,"metricName":" # short indels"},{"values":[4,11,3,10,8],"quality":"Less is better","isMain":false,"metricName":" # long indels"},{"values":[0,0,0,0,0],"quality":"Less is better","isMain":false,"metricName":"# N's"},{"values":["0.00","0.00","0.00","0.00","0.00"],"quality":"Less is better","isMain":true,"metricName":"# N's per 100 kbp"}]],["Genome statistics",[{"values":["100.000","99.998","100.000","99.998","100.000"],"quality":"More is better","isMain":true,"metricName":"Genome fraction (%)"},{"values":["1.001","1.003","1.001","1.003","1.003"],"quality":"Less is better","isMain":true,"metricName":"Duplication ratio"},{"values":["4494 + 3 part","4493 + 4 part","4494 + 3 part","4493 + 4 part","4494 + 3 part"],"quality":"More is better","isMain":true,"metricName":"# genes"},{"values":[3025485,2075336,3025483,2075332,2075390],"quality":"More is better","isMain":false,"metricName":"Largest alignment"},{"values":[4644061,4651184,4644056,4651207,4651348],"quality":"More is better","isMain":false,"metricName":"NG50"},{"values":[4644061,4651184,4644056,4651207,4651348],"quality":"More is better","isMain":false,"metricName":"NG75"},{"values":[3025485,960375,3025483,960380,960403],"quality":"More is better","isMain":false,"metricName":"NA50"},{"values":[608635,948848,608628,948827,948935],"quality":"More is better","isMain":false,"metricName":"NA75"},{"values":[3025485,960375,3025483,960380,960403],"quality":"More is better","isMain":true,"metricName":"NGA50"},{"values":[608635,948848,608628,948827,948935],"quality":"More is better","isMain":false,"metricName":"NGA75"},{"values":[1,1,1,1,1],"quality":"Less is better","isMain":false,"metricName":"LG50"},{"values":[1,1,1,1,1],"quality":"Less is better","isMain":false,"metricName":"LG75"},{"values":[1,2,1,2,2],"quality":"Less is better","isMain":false,"metricName":"LA50"},{"values":[2,3,2,3,3],"quality":"Less is better","isMain":false,"metricName":"LA75"},{"values":[1,2,1,2,2],"quality":"Less is better","isMain":false,"metricName":"LGA50"},{"values":[2,3,2,3,3],"quality":"Less is better","isMain":false,"metricName":"LGA75"}]],["Predicted genes",[]],["Reference statistics",[{"values":[4639675,4639675,4639675,4639675,4639675],"quality":"Equal","isMain":false,"metricName":"Reference length"},{"values":["50.79","50.79","50.79","50.79","50.79"],"quality":"Equal","isMain":false,"metricName":"Reference GC (%)"},{"values":[4497,4497,4497,4497,4497],"quality":"Equal","isMain":false,"metricName":"Reference genes"}]]],"minContig":500,"order":[0,1,2,3,4],"assembliesNames":["f25_d9_all","f25_d9_all_0.9g","f25_d9_all_1.1g","f25_d9_all_0.8g","f25_d9_all_1.2g"]}
{{ qualities }}
{{ mainMetrics }}
{"lists_of_lengths":[[4644061],[4651184],[4644056],[4651207],[4651348]],"filenames":["f25_d9_all","f25_d9_all_0.9g","f25_d9_all_1.1g","f25_d9_all_0.8g","f25_d9_all_1.2g"]}
{"lists_of_lengths":[[3025485,608635,572183,343359,89845,1816,1201,769,768],[2075336,960375,948848,572205,89868,1816,1199,769,768],[3025483,608628,572182,343361,89848,1816,1201,769,768],[2075332,960380,948827,572203,89866,1816,1199,769,768],[2075390,960403,948935,572203,89865,1816,1199,769,768]],"filenames":["f25_d9_all","f25_d9_all_0.9g","f25_d9_all_1.1g","f25_d9_all_0.8g","f25_d9_all_1.2g"]}
{"assemblies_lengths":[4644061,4651184,4644056,4651207,4651348],"filenames":["f25_d9_all","f25_d9_all_0.9g","f25_d9_all_1.1g","f25_d9_all_0.8g","f25_d9_all_1.2g"]}
{"reflen":4639675}
{"ref_genes_number":4497,"genes_in_contigs":{"f25_d9_all_1.2g":[4494],"f25_d9_all_0.8g":[4493],"f25_d9_all":[4494],"f25_d9_all_0.9g":[4493],"f25_d9_all_1.1g":[4494]},"filenames":["f25_d9_all","f25_d9_all_0.9g","f25_d9_all_1.1g","f25_d9_all_0.8g","f25_d9_all_1.2g"]}
{{ operonsInContigs }}
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{
"# contigs" : "is the total number of contigs in the assembly.",
"Largest contig" : "is the length of the longest contig in the assembly.",
"Total length" : "is the total number of bases in the assembly.",
"Reference length" : "is the total number of bases in the reference.",
"N50" : "is the contig length such that using longer or equal length contigs produces half (50%) of the bases of the assembly. Usually there is no value that produces exactly 50%, so the technical definition is the maximum length x such that using contigs of length at least x accounts for at least 50% of the total assembly length.",
"NG50" : "is the contig length such that using longer or equal length contigs produces half (50%) of the bases of the reference genome. This metric is computed only if a reference genome is provided.",
"N75" : "is the contig length such that using longer or equal length contigs produces 75% of the bases of the assembly. Usually there is no value that produces exactly 75%, so the technical definition is the maximum length x such that using contigs of length at least x accounts for at least 75% of the total assembly length.",
"NG75" : "is the contig length such that using longer or equal length contigs produces 75% of the bases of the reference genome. This metric is computed only if a reference genome is provided.",
"L50" : "is the minimum number of contigs that produce half (50%) of the bases of the assembly. In other words, it's the number of contigs of length at least N50.",
"LG50" : "is the minimum number of contigs that produce half (50%) of the bases of the reference genome. In other words, it's the number of contigs of length at least NG50. This metric is computed only if a reference genome is provided.",
"L75" : "is the minimum number of contigs that produce 75% of the bases of the assembly. In other words, it's the number of contigs of length at least N75.",
"LG75" : "is the minimum number of contigs that produce 75% of the bases of the reference genome. In other words, it's the number of contigs of length at least NG75. This metric is computed only if a reference genome is provided.",
"NA50" : "is N50 where the lengths of aligned blocks are counted instead of contig lengths. I.e., if a contig has a misassembly with respect to the reference, the contig is broken into smaller pieces. This metric is computed only if a reference genome is provided.",
"NGA50" : "is NG50 where the lengths of aligned blocks are counted instead of contig lengths. I.e., if a contig has a misassembly with respect to the reference, the contig is broken into smaller pieces. This metric is computed only if a reference genome is provided.",
"NA75" : "is N75 where the lengths of aligned blocks are counted instead of contig lengths. I.e., if a contig has a misassembly with respect to the reference, the contig is broken into smaller pieces. This metric is computed only if a reference genome is provided.",
"NGA75" : "is NG75 where the lengths of aligned blocks are counted instead of contig lengths. I.e., if a contig has a misassembly with respect to the reference, the contig is broken into smaller pieces. This metric is computed only if a reference genome is provided.",
"LA50" : "is L50 where aligned blocks are counted instead of contigs. I.e., if a contig has a misassembly with respect to the reference, the contig is broken into smaller pieces.",
"LGA50" : "is LG50 where aligned blocks are counted instead of contigs. I.e., if a contig has a misassembly with respect to the reference, the contig is broken into smaller pieces.",
"LA75" : "is L75 where aligned blocks are counted instead of contigs. I.e., if a contig has a misassembly with respect to the reference, the contig is broken into smaller pieces.",
"LGA75" : "is LG75 where aligned blocks are counted instead of contigs. I.e., if a contig has a misassembly with respect to the reference, the contig is broken into smaller pieces.",
"Average %IDY" : "is the average of alignment identity percent (Nucmer measure of alignment accuracy) among all contigs.",
"# misassemblies" : "is the number of positions in the assembled contigs where the left flanking sequence aligns over 1 kbp away from the right flanking sequence on the reference (relocation) or they overlap on more than 1 kbp (relocation) or flanking sequences align on different strands (inversion) or different chromosomes (translocation).",
"# misassembled contigs" : "is the number of contigs that contain misassembly events.",
"Misassembled contigs length" : "is the number of total bases contained in all contigs that have one or more misassemblies.",
"# relocations" : "is the number of relocation events among all misassembly events. Relocation is a misassembly where the left flanking sequence aligns over 1 kbp away from the right flanking sequence on the reference, or they overlap by more than 1 kbp and both flanking sequences align on the same chromosome.",
"# translocations" : "is the number of translocation events among all misassembly events. Translocation is a misassembly where the flanking sequences align on different chromosomes.",
"# inversions" : "is the number of inversion events among all misassembly events. Inversion is a misassembly where it is not a relocation and the flanking sequences align on opposite strands of the same chromosome.",
"# local misassemblies" : "is the number of local misassemblies. We define a local misassembly breakpoint as a breakpoint that satisfies these conditions:
- Two or more distinct alignments cover the breakpoint.
- The gap between left and right flanking sequences is less than 1 kbp.
- The left and right flanking sequences both are on the same strand of the same chromosome of the reference genome.