"net/http"
_ "net/http/pprof"
"os"
+ "regexp"
"runtime"
"sort"
"strings"
"git.arvados.org/arvados.git/sdk/go/arvados"
"github.com/arvados/lightning/hgvs"
"github.com/kshedden/gonpy"
- "github.com/sirupsen/logrus"
log "github.com/sirupsen/logrus"
"golang.org/x/crypto/blake2b"
)
Name: "lightning slice-numpy",
Client: arvados.NewClientFromEnv(),
ProjectUUID: *projectUUID,
- RAM: 240000000000,
- VCPUs: 64,
+ RAM: 650000000000,
+ VCPUs: 96,
Priority: *priority,
KeepCache: 2,
APIAccess: true,
var cgnames []string
var refseq map[string][]tileLibRef
+ var reftiledata = make(map[tileLibRef][]byte, 11000000)
in0, err := open(infiles[0])
if err != nil {
return 1
}
+
+ matchGenome, err := regexp.Compile(cmd.filter.MatchGenome)
+ if err != nil {
+ err = fmt.Errorf("-match-genome: invalid regexp: %q", cmd.filter.MatchGenome)
+ return 1
+ }
+
taglen := -1
DecodeLibrary(in0, strings.HasSuffix(infiles[0], ".gz"), func(ent *LibraryEntry) error {
if len(ent.TagSet) > 0 {
}
}
for _, cg := range ent.CompactGenomes {
- cgnames = append(cgnames, cg.Name)
+ if matchGenome.MatchString(cg.Name) {
+ cgnames = append(cgnames, cg.Name)
+ }
+ }
+ for _, tv := range ent.TileVariants {
+ if tv.Ref {
+ reftiledata[tileLibRef{tv.Tag, tv.Variant}] = tv.Sequence
+ }
}
return nil
})
err = fmt.Errorf("tagset not found")
return 1
}
+ if len(cgnames) == 0 {
+ err = fmt.Errorf("no genomes found matching regexp %q", cmd.filter.MatchGenome)
+ return 1
+ }
sort.Strings(cgnames)
{
}
}
- log.Info("building list of reference tiles to load") // TODO: more efficient if we had saved all ref tiles in slice0
+ log.Info("indexing reference tiles")
type reftileinfo struct {
variant tileVariantID
seqname string // chr1
reftile := map[tagID]*reftileinfo{}
for seqname, cseq := range refseq {
for _, libref := range cseq {
- reftile[libref.Tag] = &reftileinfo{seqname: seqname, variant: libref.Variant}
- }
- }
- log.Info("loading reference tiles from all slices")
- throttleCPU := throttle{Max: runtime.GOMAXPROCS(0)}
- for _, infile := range infiles {
- infile := infile
- throttleCPU.Go(func() error {
- defer log.Infof("%s: done", infile)
- f, err := open(infile)
- if err != nil {
- return err
+ reftile[libref.Tag] = &reftileinfo{
+ seqname: seqname,
+ variant: libref.Variant,
+ tiledata: reftiledata[libref],
}
- defer f.Close()
- return DecodeLibrary(f, strings.HasSuffix(infile, ".gz"), func(ent *LibraryEntry) error {
- for _, tv := range ent.TileVariants {
- if dst, ok := reftile[tv.Tag]; ok && dst.variant == tv.Variant {
- dst.tiledata = tv.Sequence
- }
- }
- return nil
- })
- })
- }
- if err = throttleCPU.Wait(); err != nil {
- return 1
+ }
}
+ throttleCPU := throttle{Max: runtime.GOMAXPROCS(0)}
log.Info("reconstructing reference sequences")
for seqname, cseq := range refseq {
seqname, cseq := seqname, cseq
for _, libref := range cseq {
rt := reftile[libref.Tag]
rt.pos = pos
+ if len(rt.tiledata) == 0 {
+ return fmt.Errorf("missing tiledata for tag %d variant %d in %s in ref", libref.Tag, libref.Variant, seqname)
+ }
pos += len(rt.tiledata) - taglen
}
return nil
return err
}
defer f.Close()
- log.Infof("reading %s", infile)
+ log.Infof("%04d: reading %s", infileIdx, infile)
err = DecodeLibrary(f, strings.HasSuffix(infile, ".gz"), func(ent *LibraryEntry) error {
for _, tv := range ent.TileVariants {
+ if tv.Ref {
+ continue
+ }
variants := seq[tv.Tag]
if len(variants) == 0 {
variants = make([]TileVariant, 100)
seq[tv.Tag] = variants
}
for _, cg := range ent.CompactGenomes {
- cgs[cg.Name] = cg
+ if matchGenome.MatchString(cg.Name) {
+ cgs[cg.Name] = cg
+ }
}
return nil
})
// TODO: filters
- log.Infof("renumber/dedup variants for tags %d-%d", tagstart, tagend)
+ log.Infof("%04d: renumber/dedup variants for tags %d-%d", infileIdx, tagstart, tagend)
variantRemap := make([][]tileVariantID, tagend-tagstart)
throttleCPU := throttle{Max: runtime.GOMAXPROCS(0)}
for tag, variants := range seq {
defer throttleCPU.Release()
count := make(map[[blake2b.Size256]byte]int, len(variants))
for _, cg := range cgs {
- idx := (tag - tagstart) * 2
- if int(idx) < len(cg.Variants) {
- count[variants[cg.Variants[idx]].Blake2b]++
- count[variants[cg.Variants[idx+1]].Blake2b]++
+ idx := int(tag-tagstart) * 2
+ if idx < len(cg.Variants) {
+ for allele := 0; allele < 2; allele++ {
+ v := cg.Variants[idx+allele]
+ if v > 0 && len(variants[v].Sequence) > 0 {
+ count[variants[v].Blake2b]++
+ }
+ }
}
}
// hash[i] will be the hash of
throttleCPU.Wait()
annotationsFilename := fmt.Sprintf("%s/matrix.%04d.annotations.csv", *outputDir, infileIdx)
- log.Infof("writing %s", annotationsFilename)
+ log.Infof("%04d: writing %s", infileIdx, annotationsFilename)
annof, err := os.Create(annotationsFilename)
if err != nil {
return err
outcol := tag - tagID(tagstart)
reftilestr := strings.ToUpper(string(rt.tiledata))
remap := variantRemap[tag-tagstart]
+ done := make([]bool, len(variants))
for v, tv := range variants {
+ v := remap[v]
+ if done[v] {
+ continue
+ } else {
+ done[v] = true
+ }
if len(tv.Sequence) < taglen || !bytes.HasSuffix(rt.tiledata, tv.Sequence[len(tv.Sequence)-taglen:]) {
continue
}
diffs, _ := hgvs.Diff(reftilestr, strings.ToUpper(string(tv.Sequence)), 0)
for _, diff := range diffs {
diff.Position += rt.pos
- fmt.Fprintf(annow, "%d,%d,%d,%s:g.%s\n", tag, outcol, remap[v], rt.seqname, diff.String())
+ fmt.Fprintf(annow, "%d,%d,%d,%s:g.%s,%s,%d,%s,%s,%s\n", tag, outcol, v, rt.seqname, diff.String(), rt.seqname, diff.Position, diff.Ref, diff.New, diff.Left)
}
}
}
}
throttleNumpyMem.Acquire()
- log.Infof("%s: preparing numpy", infile)
+ log.Infof("%04d: preparing numpy", infileIdx)
rows := len(cgnames)
cols := 2 * int(tagend-tagstart)
out := make([]int16, rows*cols)
if err != nil {
return err
}
- log.WithFields(logrus.Fields{
+ log.WithFields(log.Fields{
"filename": fnm,
"rows": rows,
"cols": cols,
- }).Info("writing numpy")
+ }).Infof("%04d: writing numpy", infileIdx)
npw.Shape = []int{rows, cols}
npw.WriteInt16(out)
err = bufw.Flush()