4363: Accept manifest_text in a non-UTF-8 encoding that is equal to its UTF-8 encoding.
[arvados.git] / crunch_scripts / split-fastq.py
index 42b8e6170230661d969ff4cda6267a78184d53e3..17aabf2930393a48d3539483d5198cab5af35631 100755 (executable)
@@ -3,6 +3,7 @@
 import arvados
 import re
 import hashlib
+import string
 
 api = arvados.api('v1')
 
@@ -13,36 +14,116 @@ manifest_text = ""
 
 inp = arvados.CollectionReader(arvados.getjobparam('reads'))
 
-prog = re.compile("(.*?)_1.fastq(.gz)?$")
+manifest_list = []
 
-manifest_text = ""
+chunking = False #arvados.getjobparam('chunking')
+
+def nextline(reader, start):
+    n = -1
+    while True:
+        r = reader.readfrom(start, 128)
+        if r == '':
+            break
+        n = string.find(r, "\n")
+        if n > -1:
+            break
+        else:
+            start += 128
+    return n
+
+# Chunk a fastq into approximately 64 MiB chunks.  Requires that the input data
+# be decompressed ahead of time, such as using decompress-all.py.  Generates a
+# new manifest, but doesn't actually move any data around.  Handles paired
+# reads by ensuring that each chunk of a pair gets the same number of records.
+#
+# This works, but in practice is so slow that potential gains in alignment
+# performance are lost in the prep time, which is why it is currently disabled.
+#
+# A better algorithm would seek to a file position a bit less than the desired
+# chunk size and then scan ahead for the next record, making sure that record
+# was matched by the read pair.
+def splitfastq(p):
+    for i in xrange(0, len(p)):
+        p[i]["start"] = 0
+        p[i]["end"] = 0
+
+    count = 0
+    recordsize = [0, 0]
+
+    global piece
+    finish = False
+    while not finish:
+        for i in xrange(0, len(p)):
+            recordsize[i] = 0
+
+        # read next 4 lines
+        for i in xrange(0, len(p)):
+            for ln in xrange(0, 4):
+                r = nextline(p[i]["reader"], p[i]["end"]+recordsize[i])
+                if r == -1:
+                    finish = True
+                    break
+                recordsize[i] += (r+1)
 
+        splitnow = finish
+        for i in xrange(0, len(p)):
+            if ((p[i]["end"] - p[i]["start"]) + recordsize[i]) >= (64*1024*1024):
+                splitnow = True
+
+        if splitnow:
+            for i in xrange(0, len(p)):
+                global manifest_list
+                print >>sys.stderr, "Finish piece ./_%s/%s (%s %s)" % (piece, p[i]["reader"].name(), p[i]["start"], p[i]["end"])
+                manifest = []
+                manifest.extend(["./_" + str(piece)])
+                manifest.extend([d[arvados.LOCATOR] for d in p[i]["reader"]._stream._data_locators])
+                manifest.extend(["{}:{}:{}".format(seg[arvados.LOCATOR]+seg[arvados.OFFSET], seg[arvados.SEGMENTSIZE], p[i]["reader"].name().replace(' ', '\\040')) for seg in arvados.locators_and_ranges(p[i]["reader"].segments, p[i]["start"], p[i]["end"] - p[i]["start"])])
+                manifest_list.append(manifest)
+                p[i]["start"] = p[i]["end"]
+            piece += 1
+        else:
+            for i in xrange(0, len(p)):
+                p[i]["end"] += recordsize[i]
+            count += 1
+            if count % 10000 == 0:
+                print >>sys.stderr, "Record %s at %s" % (count, p[i]["end"])
+
+prog = re.compile(r'(.*?)(_[12])?\.fastq(\.gz)?$')
+
+# Look for fastq files
 for s in inp.all_streams():
-    if s.name() == ".":
-        for f in s.all_files():
-            result = prog.match(f.name())
-            if result != None:
-                p = [{}, {}]
-                p[0]["reader"] = s.files()[result.group(0)]
-                p[1]["reader"] = s.files()[result.group(1) + "_2.fastq" + result.group(2)]
-                m0 = p[0]["reader"].as_manifest()[1:]
-                m1 = p[1]["reader"].as_manifest()[1:]
-                manifest_text += "./_" + str(piece) + m0
-                manifest_text += "./_" + str(piece) + m1
-                piece += 1
-
-# No pairs found so just put each fastq file into a separate directory
-if manifest_text == "":
-    for s in inp.all_streams():
-        prog = re.compile("(.*?).fastq(.gz)?$")
-        if s.name() == ".":
-            for f in s.all_files():
-                result = prog.match(f.name())
-                if result != None:
-                    p = [{}]
-                    p[0]["reader"] = s.files()[result.group(0)]
-                    m0 = p[0]["reader"].as_manifest()[1:]
-                    manifest_text += "./_" + str(piece) + m0
+    for f in s.all_files():
+        name_pieces = prog.match(f.name())
+        if name_pieces is not None:
+            if s.name() != ".":
+                # The downstream tool (run-command) only iterates over the top
+                # level of directories so if there are fastq files in
+                # directories in the input, the choice is either to forget
+                # there are directories (which might lead to name conflicts) or
+                # just fail.
+                print >>sys.stderr, "fastq must be at the root of the collection"
+                sys.exit(1)
+
+            p = None
+            if name_pieces.group(2) is not None:
+                if name_pieces.group(2) == "_1":
+                    p = [{}, {}]
+                    p[0]["reader"] = s.files()[name_pieces.group(0)]
+                    p[1]["reader"] = s.files()[name_pieces.group(1) + "_2.fastq" + (name_pieces.group(3) if name_pieces.group(3) else '')]
+            else:
+                p = [{}]
+                p[0]["reader"] = s.files()[name_pieces.group(0)]
+
+            if p is not None:
+                if chunking:
+                    splitfastq(p)
+                else:
+                    for i in xrange(0, len(p)):
+                        m = p[i]["reader"].as_manifest().split()
+                        m[0] = "./_" + str(piece)
+                        manifest_list.append(m)
                     piece += 1
 
+manifest_text = "\n".join(" ".join(m) for m in manifest_list) + "\n"
+
 arvados.current_task().set_output(manifest_text)