예제 #1
0
파일: Manifest.cs 프로젝트: abladon/canvas
 /// <summary>
 /// Output bed file of regions. Each region spans both probes and the target interval
 /// Note that the BED format uses:
 /// 0-based start position (inclusive) and 1-based end position (inclusive)
 /// which is equivalent to saying:
 /// 0-based start position (inclusive) and 0-based end position (exclusive)
 /// </summary>
 public static void WriteRegionBed(NexteraManifest manifest, string outputPath, GenomeMetadata genome)
 {
     using (BgzipOrStreamWriter writer = new BgzipOrStreamWriter(outputPath))
     {
         WriteRegionBed(manifest, writer, genome);
     }
 }
예제 #2
0
파일: Manifest.cs 프로젝트: abladon/canvas
        public static void WriteTargetBed(NexteraManifest manifest, BgzipOrStreamWriter writer, GenomeMetadata genome)
        {
            List<NexteraManifest.ManifestRegion> tempRegions = manifest.Regions;
            if (genome != null)
            {
                tempRegions = new List<NexteraManifest.ManifestRegion>(manifest.Regions);
                Dictionary<string, int> chromsomeIndexLookup = new Dictionary<string, int>();
                //generate chromsome index lookup and sort
                for (int chromosomeIndex = 0; chromosomeIndex < genome.Sequences.Count; chromosomeIndex++)
                {
                    GenomeMetadata.SequenceMetadata sequence = genome.Sequences[chromosomeIndex];
                    chromsomeIndexLookup[sequence.Name] = chromosomeIndex;
                }
                tempRegions.Sort((a, b) => a.CompareTo(b, chromsomeIndexLookup));
            }

                foreach (NexteraManifest.ManifestRegion region in tempRegions)
                {
                TargetInterval interval = region.GetTargetInterval();
                    writer.WriteLine(string.Join("\t", new[]
                    {
                        interval.ReferenceName, 
                        (interval.Begin - 1).ToString(CultureInfo.InvariantCulture), 
                        interval.End.ToString(CultureInfo.InvariantCulture),
                    region.Name //region name is needed for PUMA metrics outputs to generate .coverage.csv file
                    }));
                }
            }
예제 #3
0
파일: Manifest.cs 프로젝트: abladon/canvas
        public static void WriteRegionBed(NexteraManifest manifest, BgzipOrStreamWriter writer, GenomeMetadata genome)
        {
            List<NexteraManifest.ManifestRegion> tempRegions = manifest.Regions;
            if (genome != null)
            {
                tempRegions = new List<NexteraManifest.ManifestRegion>(manifest.Regions);
                Dictionary<string, int> chromsomeIndexLookup = new Dictionary<string, int>();
                //generate chromsome index lookup and sort
                for (int chromosomeIndex = 0; chromosomeIndex < genome.Sequences.Count; chromosomeIndex++)
                {
                    GenomeMetadata.SequenceMetadata sequence = genome.Sequences[chromosomeIndex];
                    chromsomeIndexLookup[sequence.Name] = chromosomeIndex;
                }
                tempRegions.Sort((a, b) => a.CompareTo(b, chromsomeIndexLookup));
            }

                foreach (NexteraManifest.ManifestRegion region in tempRegions)
                {
                    writer.WriteLine(string.Format("{0}\t{1}\t{2}", region.Chromosome, region.Start - 1, region.End));
                }
            }
예제 #4
0
        /// <summary>
        /// Outputs the copy number calls to a text file.
        /// </summary>
        /// <param name="outVcfPath">File to write to.</param>
        /// <param name="segments">List of segments to write out.</param>
        public static void WriteSegments(string outVcfPath, List<CanvasSegment> segments, string reference, string sampleName,
            List<string> extraHeaders, bool reportPloidy, PloidyInfo ploidy, bool reportAllSites = false, bool reportGermlineGenotype = false)
        {
            string cnvtype = null;
            string filter = null;
            // report GT for resequencing workflow and MCC for tumour-normal workflow
            if (reportGermlineGenotype && reportPloidy)
            {
                throw new Exception("WriteSegments VCF file output error: reportGermlineGenotype and reportPloidy can not be both true");
            }

            using (BgzipOrStreamWriter writer = new BgzipOrStreamWriter(outVcfPath))
            {
                // Write the VCF header:
                writer.WriteLine("##fileformat=VCFv4.1");
                writer.WriteLine("##source=Isas," + CanvasCommon.CanvasVersionInfo.NameString + " " + CanvasCommon.CanvasVersionInfo.VersionString);
                writer.WriteLine("##reference={0}", Path.Combine(reference, "genome.fa"));
                if (extraHeaders != null)
                {
                    foreach (string header in extraHeaders)
                    {
                        writer.WriteLine(header);
                    }
                }
                GenomeMetadata genome = new GenomeMetadata();
                genome.Deserialize(Path.Combine(reference, "GenomeSize.xml"));
                foreach (GenomeMetadata.SequenceMetadata chromosome in genome.Sequences)
                {
                    writer.WriteLine("##contig=<ID={0},length={1}>", chromosome.Name, chromosome.Length);
                }

                writer.WriteLine("##ALT=<ID=CNV,Description=\"Copy number variable region\">");
                writer.WriteLine("##FILTER=<ID=q10,Description=\"Quality below 10\">");
                writer.WriteLine("##FILTER=<ID=L10kb,Description=\"Length shorter than 10kb\">");
                writer.WriteLine("##INFO=<ID=SVTYPE,Number=1,Type=String,Description=\"Type of structural variant\">");
                writer.WriteLine("##INFO=<ID=END,Number=1,Type=Integer,Description=\"End position of the variant described in this record\">");
                writer.WriteLine("##INFO=<ID=CNVLEN,Number=1,Type=Integer,Description=\"Number of reference positions spanned by this CNV\">");
                if (reportGermlineGenotype)
                    writer.WriteLine("##FORMAT=<ID=GT,Number=1,Type=String,Description=\"Genotype\">");
                writer.WriteLine("##FORMAT=<ID=RC,Number=1,Type=Float,Description=\"Mean counts per bin in the region\">");
                writer.WriteLine("##FORMAT=<ID=BC,Number=1,Type=Float,Description=\"Number of bins in the region\">");
                writer.WriteLine("##FORMAT=<ID=CN,Number=1,Type=Integer,Description=\"Copy number genotype for imprecise events\">");
                if (reportPloidy)
                    writer.WriteLine("##FORMAT=<ID=MCC,Number=1,Type=Integer,Description=\"Major chromosome count (equal to copy number for LOH regions)\">");
                writer.WriteLine("#CHROM\tPOS\tID\tREF\tALT\tQUAL\tFILTER\tINFO\tFORMAT\t" + sampleName);

                SanityCheckChromosomeNames(genome, segments);

                foreach (GenomeMetadata.SequenceMetadata chromosome in genome.Sequences)
                {
                    foreach (CanvasSegment segment in segments)
                    {
                        if (segment.Chr.ToLowerInvariant() != chromosome.Name.ToLowerInvariant()) continue;
                        int referenceCN = 2;
                        if (ploidy != null) referenceCN = ploidy.GetReferenceCopyNumber(segment);
                        filter = null;
                        bool isReferenceCall = false;
                        if (segment.CopyNumber == referenceCN) isReferenceCall = true;
                        if (reportPloidy && segment.CopyNumber == 2 && segment.MajorChromosomeCount.HasValue && segment.MajorChromosomeCount != 1) isReferenceCall = false; // If we're reporting ploidy and there's LOH, this isn't a reference call.

                        // We can skip reporting of reference sites:
                        if (!reportAllSites && isReferenceCall)
                            continue;

                        if (segment.QScore < 10)
                            filter = "q10";

                        if (segment.End - segment.Begin < 10000)
                        {
                            if (filter != null)
                                filter = filter + ";L10kb";
                            else
                                filter = "L10kb";
                        }

                        if (filter == null)
                            filter = "PASS";

                        if (segment.CopyNumber < referenceCN)
                            cnvtype = "LOSS";
                        else if (segment.CopyNumber > referenceCN)
                            cnvtype = "GAIN";
                        else
                            cnvtype = "REF";

                        // The Dude abides... from vcf 4.1 spec:
                        //     If any of the ALT alleles is a symbolic allele (an angle-bracketed ID String “<ID>”) then the padding base is required and POS denotes the 
                        //     coordinate of the base preceding the polymorphism.
                        writer.Write("{0}\t{1}\tCanvas:{2}:{0}:{3}-{4}\t", segment.Chr, isReferenceCall ? segment.Begin + 1 : segment.Begin, cnvtype, segment.Begin + 1, segment.End);
                        writer.Write("N\t{0}\t{1}\t{2}\t", isReferenceCall ? "." : "<CNV>", segment.QScore, filter);
                        if (segment.copyNumber != referenceCN)
                            writer.Write("SVTYPE=CNV;");
                        else if (!isReferenceCall)
                            writer.Write("SVTYPE=LOH;");
                        if (segment.copyNumber != referenceCN || !isReferenceCall)
                            writer.Write("END={0};CNVLEN={1}", segment.End, segment.End - segment.Begin);
                        else
                            writer.Write("END={0}", segment.End);
                        //  FORMAT field
                        if (reportGermlineGenotype)
                            writer.Write("\tGT:RC:BC:CN", segment.End);
                        else
                            writer.Write("\tRC:BC:CN", segment.End);
                        if (reportPloidy && segment.MajorChromosomeCount.HasValue) writer.Write(":MCC");
                        // writing GT for resequencing workflow 
                        if (reportGermlineGenotype)
                        {
                            writer.Write("\t{0}/{1}:", segment.MajorChromosomeCount, segment.CopyNumber);
                        }
                        else
                            writer.Write("\t");
                        writer.Write("{1}:{2}:{3}", segment.End, Math.Round(segment.MeanCount, 0, MidpointRounding.AwayFromZero), segment.BinCount, segment.CopyNumber);
                        // writing MCC for tumour-normal workflow 
                        if (reportPloidy && segment.MajorChromosomeCount.HasValue)
                        {
                            writer.Write(":{0}", segment.MajorChromosomeCount);
                        }
                        writer.WriteLine();
                    }
                }
            }
        }
예제 #5
0
        /// <summary>
        /// Outputs the copy number calls to a text file.
        /// </summary>
        public static void WriteSegments(string outVcfPath, List<CanvasSegment> segments, string wholeGenomeFastaDirectory, string sampleName,
            List<string> extraHeaders, PloidyInfo ploidy, int qualityThreshold = 10)
        {
            using (BgzipOrStreamWriter writer = new BgzipOrStreamWriter(outVcfPath))
            {
                // Write the VCF header:
                writer.WriteLine("##fileformat=VCFv4.1");
                writer.WriteLine($"##source={CanvasVersionInfo.NameString} {CanvasVersionInfo.VersionString}");
                writer.WriteLine($"##reference={Path.Combine(wholeGenomeFastaDirectory, "genome.fa")}");

                foreach (string header in extraHeaders ?? new List<string>())
                {
                    writer.WriteLine(header);
                }
                GenomeMetadata genome = new GenomeMetadata();
                genome.Deserialize(Path.Combine(wholeGenomeFastaDirectory, "GenomeSize.xml"));
                foreach (GenomeMetadata.SequenceMetadata chromosome in genome.Sequences)
                {
                    writer.WriteLine($"##contig=<ID={chromosome.Name},length={chromosome.Length}>");
                }
                string qualityFilter = $"q{qualityThreshold}";
                writer.WriteLine("##ALT=<ID=CNV,Description=\"Copy number variable region\">");
                writer.WriteLine($"##FILTER=<ID={qualityFilter},Description=\"Quality below {qualityThreshold}\">");
                writer.WriteLine("##FILTER=<ID=L10kb,Description=\"Length shorter than 10kb\">");
                writer.WriteLine("##INFO=<ID=SVTYPE,Number=1,Type=String,Description=\"Type of structural variant\">");
                writer.WriteLine("##INFO=<ID=END,Number=1,Type=Integer,Description=\"End position of the variant described in this record\">");
                writer.WriteLine("##INFO=<ID=CNVLEN,Number=1,Type=Integer,Description=\"Number of reference positions spanned by this CNV\">");
                writer.WriteLine("##FORMAT=<ID=RC,Number=1,Type=Float,Description=\"Mean counts per bin in the region\">");
                writer.WriteLine("##FORMAT=<ID=BC,Number=1,Type=Float,Description=\"Number of bins in the region\">");
                writer.WriteLine("##FORMAT=<ID=CN,Number=1,Type=Integer,Description=\"Copy number genotype for imprecise events\">");
                writer.WriteLine("##FORMAT=<ID=MCC,Number=1,Type=Integer,Description=\"Major chromosome count (equal to copy number for LOH regions)\">");
                writer.WriteLine("#CHROM\tPOS\tID\tREF\tALT\tQUAL\tFILTER\tINFO\tFORMAT\t" + sampleName);

                SanityCheckChromosomeNames(genome, segments);

                foreach (GenomeMetadata.SequenceMetadata chromosome in genome.Sequences)
                {
                    foreach (CanvasSegment segment in segments)
                    {
                        if (!segment.Chr.Equals(chromosome.Name, StringComparison.OrdinalIgnoreCase)) continue;

                        int referenceCopyNumber = ploidy?.GetReferenceCopyNumber(segment) ?? 2;
                        CnvType cnvType = segment.GetCnvType(referenceCopyNumber);

                        // From vcf 4.1 spec:
                        //     If any of the ALT alleles is a symbolic allele (an angle-bracketed ID String “<ID>”) then the padding base is required and POS denotes the
                        //     coordinate of the base preceding the polymorphism.
                        string alternateAllele = cnvType.ToAltId();
                        int position = (alternateAllele.StartsWith("<") && alternateAllele.EndsWith(">")) ? segment.Begin : segment.Begin + 1;
                        writer.Write($"{segment.Chr}\t{position}\tCanvas:{cnvType.ToVcfId()}:{segment.Chr}:{segment.Begin + 1}-{segment.End}\t");

                        writer.Write($"N\t{alternateAllele}\t{segment.QScore}\t{segment.Filter}\t", alternateAllele, segment.QScore, segment.Filter);

                        if (cnvType != CnvType.Reference)
                            writer.Write($"SVTYPE={cnvType.ToSvType()};");
                        writer.Write($"END={segment.End}");
                        if (cnvType != CnvType.Reference)
                            writer.Write($";CNVLEN={segment.End - segment.Begin}");

                        //  FORMAT field
                        writer.Write("\tRC:BC:CN", segment.End);
                        if (segment.MajorChromosomeCount.HasValue)
                        {
                            writer.Write(":MCC");
                        }
                        writer.Write("\t{1}:{2}:{3}", segment.End, Math.Round(segment.MeanCount, 0, MidpointRounding.AwayFromZero), segment.BinCount, segment.CopyNumber);
                        if (segment.MajorChromosomeCount.HasValue)
                        {
                            writer.Write(":{0}", segment.MajorChromosomeCount);
                        }
                        writer.WriteLine();
                    }
                }
            }
        }