本文整理汇总了Java中htsjdk.samtools.SAMRecord.getAlignmentStart方法的典型用法代码示例。如果您正苦于以下问题:Java SAMRecord.getAlignmentStart方法的具体用法?Java SAMRecord.getAlignmentStart怎么用?Java SAMRecord.getAlignmentStart使用的例子?那么, 这里精选的方法代码示例或许可以为您提供帮助。您也可以进一步了解该方法所在类htsjdk.samtools.SAMRecord
的用法示例。
在下文中一共展示了SAMRecord.getAlignmentStart方法的11个代码示例,这些例子默认根据受欢迎程度排序。您可以为喜欢或者感觉有用的代码点赞,您的评价将有助于系统推荐出更棒的Java代码示例。
示例1: calcBAQFromHMM
import htsjdk.samtools.SAMRecord; //导入方法依赖的package包/类
public BAQCalculationResult calcBAQFromHMM(SAMRecord read, RefContentProvider refContentProvider) {
// start is alignment start - band width / 2 - size of first I element, if there is one. Stop is similar
int offset = getBandWidth() / 2;
long readStart = includeClippedBases ? read.getUnclippedStart() : read.getAlignmentStart();
long start = Math.max(readStart - offset - ReadUtils.getFirstInsertionOffset(read), 0);
long stop = (includeClippedBases ? read.getUnclippedEnd() : read.getAlignmentEnd()) + offset + ReadUtils.getLastInsertionOffset(read);
if ( stop > refContentProvider.getSamSequenceDictionary().getSequence(read.getReferenceName()).getSequenceLength() ) {
return null;
} else {
// now that we have the start and stop, get the reference sequence covering it
GenomeLoc locus = new GenomeLoc(read.getReferenceName(), read.getReferenceIndex(), (int)start, (int)stop);
byte[] refSeq = refContentProvider.getReferenceContext(locus).getBases();
return calcBAQFromHMM(read, refSeq, (int)(start - readStart));
}
}
示例2: transfer
import htsjdk.samtools.SAMRecord; //导入方法依赖的package包/类
/**
* Write the record.
*
* @param alignment SAMRecord.
*/
public BasicSamRecord transfer(final SAMRecord alignment) {
String readName = alignment.getReadName();
int flags = alignment.getFlags();
int contigId = alignment.getReferenceIndex();
if (contigId == SAMRecord.NO_ALIGNMENT_REFERENCE_INDEX) {
contigId = FAKE_CONTIG_ID;
}
String contigName = alignment.getReferenceName();
int position = alignment.getAlignmentStart();
int mapQ = alignment.getMappingQuality();
String cigar = alignment.getCigarString();
int mateContigId = alignment.getMateReferenceIndex();
if (mateContigId == SAMRecord.NO_ALIGNMENT_REFERENCE_INDEX) {
mateContigId = FAKE_CONTIG_ID;
}
String mateContigName = alignment.getMateReferenceName();
int matePosition = alignment.getMateAlignmentStart();
int inferredSize = alignment.getInferredInsertSize();
byte[] sequence = alignment.getReadString().getBytes();
byte[] quality = alignment.getBaseQualityString().getBytes();
List<SAMRecord.SAMTagAndValue> attributes = alignment.getAttributes();
List<String> encodedTags = new ArrayList<>(attributes.size());
for (SAMRecord.SAMTagAndValue attribute : attributes) {
encodedTags.add(tagCodec.encode(attribute.tag, attribute.value));
}
// 在这里统一不压缩,压缩操作是由scala代码中的执行引擎统一调配的。
return BasicSamRecord.apply(false, readName, flags, contigId, contigName, position, mapQ,
cigar, mateContigId, mateContigName, matePosition, inferredSize,
sequence, quality, encodedTags);
}
示例3: createGenomeLoc
import htsjdk.samtools.SAMRecord; //导入方法依赖的package包/类
/**
* Create a genome loc, given a read. If the read is unmapped, *and* yet the read has a contig and start position,
* then a GenomeLoc is returned for contig:start-start, otherwise an UNMAPPED GenomeLoc is returned.
*
* @param read the read from which to create a genome loc
* @return the GenomeLoc that was created
*/
public GenomeLoc createGenomeLoc(final SAMRecord read) {
if (read.getReadUnmappedFlag() && read.getReferenceIndex() == -1)
// read is unmapped and not placed anywhere on the genome
return GenomeLoc.UNMAPPED;
else {
// Use Math.max to ensure that end >= start (Picard assigns the end to reads that are entirely within an insertion as start-1)
final int end = read.getReadUnmappedFlag() ? read.getAlignmentStart() : Math.max(read.getAlignmentEnd(), read.getAlignmentStart());
return createGenomeLoc(read.getReferenceName(), read.getReferenceIndex(), read.getAlignmentStart(), end, false);
}
}
示例4: hasWellDefinedFragmentSize
import htsjdk.samtools.SAMRecord; //导入方法依赖的package包/类
/**
* Can the adaptor sequence of read be reliably removed from the read based on the alignment of
* read and its mate?
*
* @param read the read to check
* @return true if it can, false otherwise
*/
public static boolean hasWellDefinedFragmentSize(final SAMRecord read) {
if ( read.getInferredInsertSize() == 0 )
// no adaptors in reads with mates in another chromosome or unmapped pairs
return false;
if ( ! read.getReadPairedFlag() )
// only reads that are paired can be adaptor trimmed
return false;
if ( read.getReadUnmappedFlag() || read.getMateUnmappedFlag() )
// only reads when both reads are mapped can be trimmed
return false;
// if ( ! read.getProperPairFlag() )
// // note this flag isn't always set properly in BAMs, can will stop us from eliminating some proper pairs
// // reads that aren't part of a proper pair (i.e., have strange alignments) can't be trimmed
// return false;
if ( read.getReadNegativeStrandFlag() == read.getMateNegativeStrandFlag() )
// sanity check on getProperPairFlag to ensure that read1 and read2 aren't on the same strand
return false;
if ( read.getReadNegativeStrandFlag() ) {
// we're on the negative strand, so our read runs right to left
return read.getAlignmentEnd() > read.getMateAlignmentStart();
} else {
// we're on the positive strand, so our mate should be to our right (his start + insert size should be past our start)
return read.getAlignmentStart() <= read.getMateAlignmentStart() + read.getInferredInsertSize();
}
}
示例5: filterOut
import htsjdk.samtools.SAMRecord; //导入方法依赖的package包/类
@Override
public boolean filterOut(SAMRecord read) {
return read.getAlignmentStart() <= 0 || ((GATKSAMRecord)read).getSoftStart() <= 0;
}
示例6: filterOut
import htsjdk.samtools.SAMRecord; //导入方法依赖的package包/类
@Override
public boolean filterOut(SAMRecord read) {
return read.getReadUnmappedFlag() || read.getAlignmentStart() == SAMRecord.NO_ALIGNMENT_START;
}
示例7: filterOut
import htsjdk.samtools.SAMRecord; //导入方法依赖的package包/类
@Override
public boolean filterOut(SAMRecord read) {
return read.getAlignmentStart() < refContentProvider.getOriginStartCoordinate()
|| read.getAlignmentStart() > refContentProvider.getOriginEndCoordinate();
}
示例8: create
import htsjdk.samtools.SAMRecord; //导入方法依赖的package包/类
/**
* Generic algorithm that takes an iterable over T objects, a getter routine to extract the reads in T,
* and returns a FragmentCollection that contains the T objects whose underlying reads either overlap (or
* not) with their mate pairs.
*
* @param readContainingObjects An iterator of objects that contain GATKSAMRecords
* @param nElements the number of elements to be provided by the iterator, which is usually known upfront and
* greatly improves the efficiency of the fragment calculation
* @param getter a helper function that takes an object of type T and returns is associated GATKSAMRecord
* @param <T>
* @return a fragment collection
*/
private static <T> FragmentCollection<T> create(final Iterable<T> readContainingObjects, final int nElements, final ReadGetter<T> getter) {
Collection<T> singletons = null;
Collection<List<T>> overlapping = null;
Map<String, T> nameMap = null;
int lastStart = -1;
// build an initial map, grabbing all of the multi-read fragments
for ( final T p : readContainingObjects ) {
final SAMRecord read = getter.get(p);
if ( read.getAlignmentStart() < lastStart ) {
throw new IllegalArgumentException(String.format(
"FragmentUtils.create assumes that the incoming objects are ordered by " +
"SAMRecord alignment start, but saw a read %s with alignment start " +
"%d before the previous start %d", read.getSAMString(), read.getAlignmentStart(), lastStart));
}
lastStart = read.getAlignmentStart();
final int mateStart = read.getMateAlignmentStart();
if ( mateStart == 0 || mateStart > read.getAlignmentEnd() ) {
// if we know that this read won't overlap its mate, or doesn't have one, jump out early
if ( singletons == null ) singletons = new ArrayList<T>(nElements); // lazy init
singletons.add(p);
} else {
// the read might overlap it's mate, or is the rightmost read of a pair
final String readName = read.getReadName();
final T pe1 = nameMap == null ? null : nameMap.get(readName);
if ( pe1 != null ) {
// assumes we have at most 2 reads per fragment
if ( overlapping == null ) overlapping = new ArrayList<List<T>>(); // lazy init
overlapping.add(Arrays.asList(pe1, p));
nameMap.remove(readName);
} else {
if ( nameMap == null ) nameMap = new HashMap<String, T>(nElements); // lazy init
nameMap.put(readName, p);
}
}
}
// add all of the reads that are potentially overlapping but whose mate never showed
// up to the oneReadPile
if ( nameMap != null && ! nameMap.isEmpty() ) {
if ( singletons == null )
singletons = nameMap.values();
else
singletons.addAll(nameMap.values());
}
return new FragmentCollection<T>(singletons, overlapping);
}
示例9: noReadCanMoveBefore
import htsjdk.samtools.SAMRecord; //导入方法依赖的package包/类
private boolean noReadCanMoveBefore(int pos, SAMRecord addedRead) {
return pos + 2 * MAX_POS_MOVE_ALLOWED < addedRead.getAlignmentStart();
}
示例10: isReadUnmapped
import htsjdk.samtools.SAMRecord; //导入方法依赖的package包/类
/**
* Due to (unfortunate) multiple ways to indicate that read is unmapped allowed by SAM format
* specification, one may need this convenience shortcut. Checks both 'read unmapped' flag and
* alignment reference index/start.
*
* Our life would be so much easier if all sam files followed the specs. In reality,
* sam files (including those generated by maq or bwa) miss headers altogether. When
* reading such a SAM file, reference name is set, but since there is no sequence dictionary,
* null is always returned for referenceIndex. Let's be paranoid here, and make sure that
* we do not call the read "unmapped" when it has only reference name set with ref. index missing
* or vice versa.
*
* @param r a non-null record
* @return true if read is unmapped
*/
public static boolean isReadUnmapped(final SAMRecord r) {
if ( r == null )
throw new IllegalArgumentException("Read cannot be null");
return r.getReadUnmappedFlag() ||
!((r.getReferenceIndex() != null && r.getReferenceIndex() != SAMRecord.NO_ALIGNMENT_REFERENCE_INDEX ||
r.getReferenceName() != null && !r.getReferenceName().equals(SAMRecord.NO_ALIGNMENT_REFERENCE_NAME)) &&
r.getAlignmentStart() != SAMRecord.NO_ALIGNMENT_START);
}
示例11: getAdaptorBoundary
import htsjdk.samtools.SAMRecord; //导入方法依赖的package包/类
/**
* Finds the adaptor boundary around the read and returns the first base inside the adaptor that is closest to
* the read boundary. If the read is in the positive strand, this is the first base after the end of the
* fragment (Picard calls it 'insert'), if the read is in the negative strand, this is the first base before the
* beginning of the fragment.
*
* There are two cases we need to treat here:
*
* 1) Our read is in the reverse strand :
*
* <----------------------| *
* |--------------------->
*
* in these cases, the adaptor boundary is at the mate start (minus one)
*
* 2) Our read is in the forward strand :
*
* |----------------------> *
* <----------------------|
*
* in these cases the adaptor boundary is at the start of the read plus the inferred insert size (plus one)
*
* @param read the read being tested for the adaptor boundary
* @return the reference coordinate for the adaptor boundary (effectively the first base IN the adaptor, closest to the read.
* CANNOT_COMPUTE_ADAPTOR_BOUNDARY if the read is unmapped or the mate is mapped to another contig.
*/
public static int getAdaptorBoundary(final SAMRecord read) {
if ( ! hasWellDefinedFragmentSize(read) ) {
return CANNOT_COMPUTE_ADAPTOR_BOUNDARY;
} else if ( read.getReadNegativeStrandFlag() ) {
return read.getMateAlignmentStart() - 1; // case 1 (see header)
} else {
final int insertSize = Math.abs(read.getInferredInsertSize()); // the inferred insert size can be negative if the mate is mapped before the read (so we take the absolute value)
return read.getAlignmentStart() + insertSize + 1; // case 2 (see header)
}
}