trp.addTemplates([input,ctl],160) # Add a template with stock concentration 80nM
else:
reagents=Sample.getAllOnPlate(Experiment.REAGENTPLATE)
for r in reagents:
if r.volume<0:
r.initvolume=-r.volume+20
Sample.clearall()
# Round 1 (Keep uncleaved +theo)
t71=trp.runT7(theo=[False,True,False],src=[input,input,ctl],tgt=[],vol=18,srcdil=80.0/24)
sv1t7=trp.saveSamps(src=t71,tgt=[],vol=10,dil=4)
rt1=trp.runRT(pos=[True,True,True ],src=t71,tgt=[],vol=22,srcdil=2)
trp.diluteInPlace(tgt=rt1,dil=2)
sv1rt=trp.saveSamps(src=rt1,tgt=[],vol=15,dil=2)
pcr1=trp.runPCR(prefix=[srcprefix],src=rt1[1],tgt=[],vol=50,srcdil=4)
trp.diluteInPlace(tgt=pcr1,dil=3)
sv1pcr=trp.saveSamps(src=pcr1,tgt=["R1"],vol=125,dil=1)
# Round 2 (-theo, Ligate, keep cleaved)
t72=trp.runT7(theo=[False,True],src=sv1pcr+sv1pcr,tgt=[],vol=17,srcdil=80.0/24)
sv2t7=trp.saveSamps(src=t72,tgt=[],vol=7,dil=4)
rt2=trp.runRT(pos=[True for i in t72+sv1t7]+[False for i in t72+sv1t7],src=t72+sv1t7+t72+sv1t7,tgt=[],vol=[12]+[9 for s in t72[1:]+sv1t7+t72+sv1t7],srcdil=2)
trp.diluteInPlace(tgt=rt2,dil=2)
lig2=trp.runLig(prefix=prodprefix,src=rt2+sv1rt,tgt=[],vol=[30]+[16 for s in rt2[1:]+sv1rt],srcdil=3)
qsamps=lig2+sv1t7+sv2t7 # Samples for QPCR
diltolig=[24 for s in t72]+[24*4 for s in sv1t7]+[24 for s in t72]+[24*4 for s in sv1t7]+[16 for s in sv1rt]+[8 for s in sv1t7]+[8 for s in sv2t7] # Their dilution so far from the T7 product point (before stop added)
dilneeded=[20000/d for d in diltolig]
qdil1=[max(50,math.sqrt(d)) for d in dilneeded] # Split dilution equally, but don't use more than 3ul in first step
qdil2=[dilneeded[i]/qdil1[i] for i in range(len(qdil1))] # Whatever remains
qpcrdil1=trp.runQPCRDIL(src=qsamps,tgt=[],vol=150,srcdil=qdil1) # First dilution before starting PCR (so the rest of the QPCR setup can be done while PCR is running)
# Round 1 (Keep cleaved -theo)
print "***** Round 1 T7 *****"
t71=trp.runT7New(theo=[False for i in inputs]+[True for i in inputs],src=inputs+inputs,tgt=[],vol=10,srcdil=10.0/3)
sv1t7=trp.saveSamps(src=t71,vol=3,dil=25,plate=trp.e.DILPLATE)
rt1=trp.runRT(pos=True,src=t71,tgt=[],vol=5,srcdil=2)
trp.diluteInPlace(tgt=rt1,dil=4)
lig1=trp.runLig(prefix="B",src=rt1,tgt=[],vol=10,srcdil=3)
trp.diluteInPlace(tgt=lig1,dil=5)
# Save in dilution plate
sv1lig=trp.saveSamps(src=lig1,vol=20,dil=5,plate=trp.e.DILPLATE)
# Only need to PCR -theo case, cleaved
pcr1=trp.runPCR(prefix="B",src=lig1[0:len(inputs)],tgt=["%s.c"%i for i in inputs],vol=25,srcdil=4,ncycles=cycles)
trp.diluteInPlace(tgt=pcr1,dil=3)
sv1pcr=trp.saveSamps(src=pcr1,tgt=[], vol=50,dil=1)
# Round 2 (Keep uncleaved +theo)
print "***** Round 2 T7 *****"
in2=pcr1+["Neg"]
t72=trp.runT7New(theo=[True for i in in2]+[False for i in in2],src=in2+in2,tgt=["%s.T2+"%i for i in in2]+["%s.T2-"%i for i in in2],vol=10,srcdil=10.0/3)
sv2t7=trp.saveSamps(src=t72,vol=3,dil=25,plate=trp.e.DILPLATE)
rt2=trp.runRT(pos=True,src=t72,tgt=[],vol=5,srcdil=2)
trp.diluteInPlace(tgt=rt2,dil=4)
lig2=trp.runLig(prefix="A",src=rt2,tgt=[],vol=10,srcdil=3)
trp.diluteInPlace(tgt=lig2,dil=5)
sv2lig=trp.saveSamps(src=lig2,vol=20,dil=5,plate=trp.e.DILPLATE)
input = templates
for round in range(ndblrounds):
# Round 1 (Keep uncleaved +theo)
t71 = trp.runT7(theo=True, src=input, vol=12, srcdil=10.0 / 3, dur=15)
rt1 = trp.runRT(pos=True, src=t71, vol=10, srcdil=2)
t71 = trp.diluteInPlace(tgt=t71, dil=5) # Dilute more to conserve
rt1 = trp.diluteInPlace(tgt=rt1, dil=3.5)
# Save RT product so can do ligation during 2nd round
sv1rt = trp.saveSamps(src=rt1, vol=8, dil=3, plate=trp.e.DILPLATE)
prodbase = "R%d-%c" % (firstround + round * 2, currprefix)
pcr1 = trp.runPCR(prefix=currprefix,
src=rt1,
tgt=[prodbase, prodbase + "-spike"],
vol=pcrvol,
srcdil=4,
ncycles=cycles1)
pcr1 = trp.diluteInPlace(tgt=pcr1, dil=2)
eppie = trp.saveSamps(src=pcr1,
tgt=[prodbase + ".D3", prodbase + "-spike.D3"],
vol=26,
dil=3,
plate=trp.e.EPPENDORFS)
# And save in dilution plate for qPCR (will need 400x dilution from this point) (also eppie may be removed before end)
pcrsave = pcrsave + trp.saveSamps(
src=eppie, vol=5, dil=20, plate=trp.e.DILPLATE)
# Round 2 (-theo, Ligate, keep cleaved)
t72 = trp.runT7(theo=False, src=pcr1, vol=12, srcdil=10.0 / 3)
t71=trp.runT7(theo=[True],src=input,vol=[10],srcdil=10.0/3,dur=15)
t71s=findsamps(t71)[0]
trp.e.waitpgm()
trp.e.w.userprompt("Check T7 volume in %s, should be %.1f ul"%(t71s.plate.wellname(t71s.well),t71s.volume))
t7all=t7all+t71
rt1=trp.runRT(pos=[True],src=t71,vol=[10],srcdil=2)
rt1s=findsamps(rt1)[0]
trp.e.waitpgm()
trp.e.w.userprompt("Check RT volume in %s, should be %.1f ul"%(rt1s.plate.wellname(rt1s.well),rt1s.volume))
trp.diluteInPlace(tgt=t71,dil=5) # Dilute more to conserve
trp.diluteInPlace(tgt=rt1,dil=3)
if doqpcr:
sv=sv+trp.saveSamps(src=rt1,vol=8,dil=5)
svligtype=svligtype+[altprefix]
svdil=svdil+[2*2*3*5]
pcr1=trp.runPCR(prefix=[currprefix],src=rt1,vol=25,srcdil=4,ncycles=cycles1)
pcr1s=findsamps(pcr1)[0]
trp.e.waitpgm()
trp.e.w.userprompt("Check PCR volume in %s, should be %.1f ul"%(pcr1s.plate.wellname(pcr1s.well),pcr1s.volume))
trp.diluteInPlace(tgt=pcr1,dil=6)
#sv1pcr=trp.saveSamps(src=pcr1,tgt=["R%d-%c"%(firstround+round*2,currprefix)],vol=125,dil=1,plate=trp.e.EPPENDORFS)
# # Round 2 (-theo, Ligate, keep cleaved)
# t72=trp.runT7(theo=[False],src=sv1pcr,vol=10,srcdil=10.0/3)
# t7all=t7all+t72
# rt2=trp.runRT(pos=True,src=t72,vol=[10],srcdil=2)
# trp.diluteInPlace(tgt=t72,dil=5) # Dilute more to conserve
# trp.diluteInPlace(tgt=rt2,dil=3)
# if doqpcr:
# sv=sv+trp.saveSamps(src=rt2,vol=8,dil=5)
# svligtype=svligtype+[altprefix]
for r in reagents:
if r.volume < 0:
r.initvolume = -r.volume + 20
Sample.clearall()
# Round 1 (Keep uncleaved +theo)
t71 = trp.runT7New(theo=True,
src=inputs,
tgt=["%s.T1+" % i for i in inputs],
vol=10,
srcdil=10.0 / 3,
dur=30)
trp.diluteInPlace(tgt=t71, dil=5)
rt1 = trp.runRT(pos=True, src=t71, tgt=[], vol=5, srcdil=2)
trp.diluteInPlace(tgt=rt1, dil=4)
pcr1 = trp.runPCR(prefix=srcprefix, src=rt1, tgt=[], vol=25, srcdil=4)
trp.diluteInPlace(tgt=pcr1, dil=3)
sv1pcr = trp.saveSamps(src=pcr1,
tgt=["%s.R1" % i for i in inputs],
vol=55,
dil=1)
# Round 2 (both rounds, +/-theo, Ligate, keep cleaved)
r2in = sv1pcr + inputs
t72 = trp.runT7New(theo=[False for i in r2in] + [True for i in r2in],
src=r2in + r2in,
tgt=[],
vol=10,
srcdil=10.0 / 3)
trp.diluteInPlace(tgt=t72, dil=5)
sv2t7 = trp.saveSamps(src=t72, vol=10, dil=10, plate=trp.e.DILPLATE)
srcdil=10.0 / 3)
sv1t7 = trp.saveSamps(src=t71, vol=3, dil=25, plate=trp.e.DILPLATE)
rt1 = trp.runRT(pos=True, src=t71, tgt=[], vol=5, srcdil=2)
trp.diluteInPlace(tgt=rt1, dil=4)
lig1 = trp.runLig(prefix="B", src=rt1, tgt=[], vol=10, srcdil=3)
trp.diluteInPlace(tgt=lig1, dil=5)
# Save in dilution plate
sv1lig = trp.saveSamps(src=lig1, vol=20, dil=5, plate=trp.e.DILPLATE)
# Only need to PCR -theo case, cleaved
pcr1 = trp.runPCR(prefix="B",
src=lig1[0:len(inputs)],
tgt=["%s.c" % i for i in inputs],
vol=25,
srcdil=4,
ncycles=cycles)
trp.diluteInPlace(tgt=pcr1, dil=3)
sv1pcr = trp.saveSamps(src=pcr1, tgt=[], vol=50, dil=1)
# Round 2 (Keep uncleaved +theo)
print "***** Round 2 T7 *****"
in2 = pcr1 + ["Neg"]
t72 = trp.runT7New(theo=[True for i in in2] + [False for i in in2],
src=in2 + in2,
tgt=["%s.T2+" % i
for i in in2] + ["%s.T2-" % i for i in in2],
vol=10,
srcdil=10.0 / 3)
sv2t7 = trp.saveSamps(src=t72, vol=3, dil=25, plate=trp.e.DILPLATE)
vol=12,
srcdil=10.0 / 3,
dur=15)
t7all = t7all + t71
rt1 = trp.runRT(pos=[True], src=t71, vol=[10], srcdil=2)
trp.diluteInPlace(tgt=t71, dil=5) # Dilute more to conserve
trp.diluteInPlace(
tgt=rt1, dil=9
) # Dilute same as combined RT+Ligation steps in second half of double-round, reduce inhibition of PCR
if doqpcr:
sv = sv + trp.saveSamps(src=rt1, vol=8, dil=5)
svligtype = svligtype + [altprefix]
svdil = svdil + [2 * 2 * 3 * 5]
pcr1 = trp.runPCR(prefix=[currprefix],
src=rt1,
vol=25,
srcdil=4,
ncycles=cycles1)
trp.diluteInPlace(tgt=pcr1, dil=6)
sv1pcr = trp.saveSamps(
src=pcr1,
tgt=["R%d-%c" % (firstround + round * 2, currprefix)],
vol=125,
dil=1,
plate=trp.e.EPPENDORFS)
# Round 2 (-theo, Ligate, keep cleaved)
t72 = trp.runT7(theo=[False], src=sv1pcr, vol=12, srcdil=10.0 / 3)
t7all = t7all + t72
rt2 = trp.runRT(pos=True, src=t72, vol=[10], srcdil=2)
trp.diluteInPlace(tgt=t72, dil=5) # Dilute more to conserve
ligsave2=[]
pcrsave=[]
input=templates
for round in range(ndblrounds):
# Round 1 (Keep uncleaved +theo)
t71=trp.runT7(theo=True,src=input,vol=12,srcdil=10.0/3,dur=15)
rt1=trp.runRT(pos=True,src=t71,vol=10,srcdil=2)
t71=trp.diluteInPlace(tgt=t71,dil=5) # Dilute more to conserve
rt1=trp.diluteInPlace(tgt=rt1,dil=3.5)
# Save RT product so can do ligation during 2nd round
sv1rt=trp.saveSamps(src=rt1,vol=8,dil=3,plate=trp.e.DILPLATE)
prodbase="R%d-%c"%(firstround+round*2,currprefix)
pcr1=trp.runPCR(prefix=currprefix,src=rt1,tgt=[prodbase,prodbase+"-spike"],vol=pcrvol,srcdil=4,ncycles=cycles1)
pcr1=trp.diluteInPlace(tgt=pcr1,dil=2)
eppie=trp.saveSamps(src=pcr1,tgt=[prodbase+".D3",prodbase+"-spike.D3"],vol=26,dil=3,plate=trp.e.EPPENDORFS)
# And save in dilution plate for qPCR (will need 400x dilution from this point) (also eppie may be removed before end)
pcrsave=pcrsave+trp.saveSamps(src=eppie,vol=5,dil=20, plate=trp.e.DILPLATE)
# Round 2 (-theo, Ligate, keep cleaved)
t72=trp.runT7(theo=False,src=pcr1,vol=12,srcdil=10.0/3)
rt2=trp.runRT(pos=True,src=t72,vol=10,srcdil=2)
t72=trp.diluteInPlace(tgt=t72,dil=5) # Dilute more to conserve
rt2=trp.diluteInPlace(tgt=rt2,dil=3)
# Swap prefixes
altprefix=currprefix
if currprefix=="B":
if r.volume < 0:
r.initvolume = -r.volume + 20
Sample.clearall()
# Round 1 (Keep uncleaved +theo)
t71 = trp.runT7New(theo=True, src=inputs, tgt=["%s.T1+" % i for i in inputs], vol=10, srcdil=10.0 / 3, dur=30)
trp.diluteInPlace(tgt=t71, dil=5)
rt1 = trp.runRT(pos=True, src=t71, tgt=[], vol=5, srcdil=2)
trp.diluteInPlace(tgt=rt1, dil=4)
rtconc = tmplConc * 3.0 / 10.0 * rnagain / (2 * 5 * 2 * 4 * 4) # Expected concentration of ligation product here
cycles = math.ceil(math.log(endconc / rtconc, pcreff))
# Amplify to end of exponential phase
print "PCR input conc=%.3g pM, PCR cycles=%.1f, End Conc=%.0f nM" % (rtconc * 1e12, cycles, endconc * 1e9)
pcr1 = trp.runPCR(prefix=srcprefix, src=rt1, tgt=[], vol=25, srcdil=4, ncycles=cycles)
trp.diluteInPlace(tgt=pcr1, dil=3)
sv1pcr = trp.saveSamps(src=pcr1, tgt=["%s.R1" % i for i in inputs], vol=55, dil=1)
# Round 2 (both rounds, +/-theo, Ligate, keep cleaved)
r2in = sv1pcr + inputs
t72 = trp.runT7New(
theo=[False for i in r2in] + [True for i in r2in], src=r2in + r2in, tgt=[], vol=10, srcdil=10.0 / 3
)
trp.diluteInPlace(tgt=t72, dil=5)
sv2t7 = trp.saveSamps(src=t72, vol=10, dil=10, plate=trp.e.DILPLATE)
rt2 = trp.runRT(pos=True, src=t72, tgt=[], vol=5, srcdil=2)
trp.diluteInPlace(tgt=rt2, dil=4)
lig2 = trp.runLig(prefix=prodprefix, src=rt2, tgt=[], vol=10, srcdil=3)
trp.diluteInPlace(tgt=lig2, dil=5)
qsamps = lig2 + sv2t7 # Samples for QPCR
svligtype=[]
svdil=[]
t7all=[]
for round in range(ndblrounds):
# Round 1 (Keep uncleaved +theo)
t71=trp.runT7(theo=[True],src=input,vol=12,srcdil=10.0/3,dur=15)
t7all=t7all+t71
rt1=trp.runRT(pos=[True],src=t71,vol=[10],srcdil=2)
trp.diluteInPlace(tgt=t71,dil=5) # Dilute more to conserve
trp.diluteInPlace(tgt=rt1,dil=9) # Dilute same as combined RT+Ligation steps in second half of double-round, reduce inhibition of PCR
if doqpcr:
sv=sv+trp.saveSamps(src=rt1,vol=8,dil=5)
svligtype=svligtype+[altprefix]
svdil=svdil+[2*2*3*5]
pcr1=trp.runPCR(prefix=[currprefix],src=rt1,vol=25,srcdil=4,ncycles=cycles1)
trp.diluteInPlace(tgt=pcr1,dil=6)
sv1pcr=trp.saveSamps(src=pcr1,tgt=["R%d-%c"%(firstround+round*2,currprefix)],vol=125,dil=1,plate=trp.e.EPPENDORFS)
# Round 2 (-theo, Ligate, keep cleaved)
t72=trp.runT7(theo=[False],src=sv1pcr,vol=12,srcdil=10.0/3)
t7all=t7all+t72
rt2=trp.runRT(pos=True,src=t72,vol=[10],srcdil=2)
trp.diluteInPlace(tgt=t72,dil=5) # Dilute more to conserve
trp.diluteInPlace(tgt=rt2,dil=3)
if doqpcr:
sv=sv+trp.saveSamps(src=rt2,vol=8,dil=5)
svligtype=svligtype+[altprefix]
svdil=svdil+[2*2*3*5]
altprefix=currprefix
if currprefix=="B":
