This isn't Samarth's assembly, but a test run I did on the side.
It's a different assembly than the one he presented at GI2014, I naively inputted his HGAP-corrected reads and ran with:

fastqToCA -technology pacbio-corrected -libraryname $libname -reads $input > ca_assembly.frg
runCA ca_assembly.frg -p $libname -d `pwd`/tmp

I recall that samarth did some post-filtering on the assembly and maybe other pre-filtering. Mine is way bigger (159 Mbp instead of expected 50 Mbp), and smaller NG50 (15 kbp).

[rxc48@brubeck celera_corrected_5kbp_filtered]$ cat ca_assembly.gkpStore.info
libIID  bgnIID  endIID  active  deleted mated   totLen  clrLen  libName
0       1       636424  636424  0       0       2338694435      2338694435      GLOBAL
0       0       0       0       0       0       0       0       LegacyUnmatedReads
1       1       636424  636424  0       0       2338694435      2338694435      ca_assembly


[rxc48@brubeck celera_corrected_5kbp_filtered]$ cat ca_assembly.gkpStore.err

Starting file '/scratch/rayan/ca_assembly.frg'.

Processing SINGLE-ENDED SANGER QV encoding reads from:
      '/scratch/rayan/data/corrected_5kbp_filtered_female.fastq'


GKP finished with no alerts or errors.