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{"subreports":[],"report":[["Genome statistics",[{"values":["98.291"],"quality":"More is better","isMain":true,"metricName":"Genome fraction (%)"},{"values":["1.039"],"quality":"Less is better","isMain":true,"metricName":"Duplication ratio"},{"values":["43 + 16 part"],"quality":"More is better","isMain":true,"metricName":"# genomic features"},{"values":[16110],"quality":"More is better","isMain":true,"metricName":"Largest alignment"},{"values":[30285],"quality":"More is better","isMain":true,"metricName":"Total aligned length"},{"values":[16248],"quality":"More is better","isMain":false,"metricName":"NG50"},{"values":[3419],"quality":"More is better","isMain":false,"metricName":"NG75"},{"values":[16110],"quality":"More is better","isMain":true,"metricName":"NGA50"},{"values":[3205],"quality":"More is better","isMain":false,"metricName":"NGA75"},{"values":[1],"quality":"Less is better","isMain":false,"metricName":"LG50"},{"values":[3],"quality":"Less is better","isMain":false,"metricName":"LG75"},{"values":[1],"quality":"Less is better","isMain":true,"metricName":"LGA50"},{"values":[3],"quality":"Less is better","isMain":false,"metricName":"LGA75"}]],["Reads mapping",[]],["Misassemblies",[{"values":[1],"quality":"Less is better","isMain":true,"metricName":"# misassemblies"},{"values":[0],"quality":"Less is better","isMain":false,"metricName":" # 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indels (<= 5 bp)"},{"values":[0],"quality":"Less is better","isMain":false,"metricName":" # indels (> 5 bp)"},{"values":[0],"quality":"Less is better","isMain":false,"metricName":"# N's"},{"values":["0.00"],"quality":"Less is better","isMain":true,"metricName":"# N's per 100 kbp"}]],["Statistics without reference",[{"values":[30],"quality":"Equal","isMain":true,"metricName":"# contigs"},{"values":[30],"quality":"Equal","isMain":false,"metricName":"# contigs (>= 0 bp)"},{"values":[20],"quality":"Equal","isMain":false,"metricName":"# contigs (>= 1000 bp)"},{"values":[1],"quality":"Equal","isMain":false,"metricName":"# contigs (>= 5000 bp)"},{"values":[1],"quality":"Equal","isMain":false,"metricName":"# contigs (>= 10000 bp)"},{"values":[0],"quality":"Equal","isMain":false,"metricName":"# contigs (>= 25000 bp)"},{"values":[0],"quality":"Equal","isMain":false,"metricName":"# contigs (>= 50000 bp)"},{"values":[16248],"quality":"More is better","isMain":true,"metricName":"Largest contig"},{"values":[61636],"quality":"More is better","isMain":true,"metricName":"Total length"},{"values":[61636],"quality":"More is better","isMain":false,"metricName":"Total length (>= 0 bp)"},{"values":[53606],"quality":"More is better","isMain":true,"metricName":"Total length (>= 1000 bp)"},{"values":[16248],"quality":"More is better","isMain":false,"metricName":"Total length (>= 5000 bp)"},{"values":[16248],"quality":"More is better","isMain":true,"metricName":"Total length (>= 10000 bp)"},{"values":[0],"quality":"More is better","isMain":false,"metricName":"Total length (>= 25000 bp)"},{"values":[0],"quality":"More is better","isMain":true,"metricName":"Total length (>= 50000 bp)"},{"values":[2603],"quality":"More is better","isMain":false,"metricName":"N50"},{"values":[1452],"quality":"More is better","isMain":false,"metricName":"N75"},{"values":[6],"quality":"Less is better","isMain":false,"metricName":"L50"},{"values":[14],"quality":"Less is better","isMain":false,"metricName":"L75"},{"values":["44.28"],"quality":"Equal","isMain":false,"metricName":"GC (%)"}]],["K-mer-based statistics",[]],["Predicted genes",[]],["Similarity statistics",[{"values":[0],"quality":"Equal","isMain":false,"metricName":"# similar correct contigs"},{"values":[0],"quality":"Equal","isMain":false,"metricName":"# similar misassembled blocks"}]],["Reference statistics",[{"values":[29903],"quality":"Equal","isMain":false,"metricName":"Reference length"},{"values":[1],"quality":"Equal","isMain":false,"metricName":"Reference fragments"},{"values":["37.97"],"quality":"Equal","isMain":false,"metricName":"Reference GC (%)"},{"values":[59],"quality":"Equal","isMain":false,"metricName":"Reference genomic features"}]]],"referenceName":"NC_045512.2","date":"13 May 2021, Thursday, 23:04:12","subreferences":[],"minContig":500,"order":[0],"assembliesNames":["CV45_contigs"]}
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{{ krona }}
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{"links_names":["View in Icarus contig browser"],"links":["icarus_viewers/alignment_viewer.html"]}
{
"# 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.",
"# contigs (>= 0 bp)" : "is the total number of contigs in the assembly that have size greater than or equal to 0 bp.",
"Total length (>= 0 bp)" : "is the total number of bases in the contigs having size greater than or equal to 0 bp.",
"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).",
"# large block misassemblies" : "is the number of misassemblies between alignments with length greater than or equal to 3 kbp and with the misassembly threshold equal to 5 kbp (instead of default 1 kbp for regular misassemblies).",
"# 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.",
"# interspecies translocations" : "is the number of interspecies translocation events among all misassembly events. Interspecies translocation is a misassembly where the flanking sequences align on different references (based on alignments to the combined reference).",
"# 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.",
"# large relocations" : "is the number of relocation events among all large block misassemblies. Relocation is a misassembly where the left flanking sequence aligns over 5 kbp away from the right flanking sequence on the reference, or they overlap by more than 5 kbp and both flanking sequences align on the same chromosome.",
"# large translocations" : "is the number of translocation events among all large block misassemblies. Translocation is a misassembly where the flanking sequences align on different chromosomes.",
"# large i/s translocations" : "is the number of interspecies translocation events among all large block misassemblies. Interspecies translocation is a misassembly where the flanking sequences align on different references (based on alignments to the combined reference).",
"# large inversions" : "is the number of inversion events among all large block misassemblies. 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 the misassembly threshold (1 kbp by default).
- The left and right flanking sequences both are on the same strand of the same chromosome of the reference genome.
- There are two misassembly breakpoints of the same type around a short alignment (less than 7 kbp by default)
- The gap between two long flanking sequences on the sides of the short alignment is less than 7 kbp.
- The long flanking sequences both are on the same strand of the same chromosome of the reference genome.