Anyone has any ideas? I'll appreciate it. On Wed, Feb 12, 2014 at 12:06 PM, Camila M. <kamynz16@xxxxxxxxx> wrote: > Hello All, > > As I said before, I'm doing a lot of Miras by groups of 500 Miras. I have > 17 lists with 500 manifest files each. > > I thougth that I didn't have any problem with the first 1500 Miras (with > the first 3 lists). However, I couldn't assembly 28 contigs of list 1, 29 > contigs of list 2, and 24 contigs of list 3. > > Mainly, I got these two error messages: > > 1) Thrown: void HashStatistics::loadHashStatisticsFile(string & > hashstatfilename, uint8 basesperhash) > > 2) Thrown: void Assembly::dumpSomeStatistics() > > > One of those manifest looks like this: > > project = comp4715_c0_seq1.mira > job = est,denovo,accurate > parameters = -GE:not=1 -NW:cmrnl=no -OUTPUT:output_result_html=yes > > readgroup = comp4715_c0_seq1._library_1 > data = > /home/ABTLUS/maria.villa/RNASeq_Pseudozyma/read_by_contig/comp4715_c0_seq1_Glicose_1_ACTTGA_merge_R1_001.fastq > /home/ABTLUS/maria.villa/RNASeq_Pseudozyma/read_by_contig/comp4715_c0_seq1_Glicose_1_ACTTGA_merge_R2_001.fastq > technology = solexa > strain = pseudozyma > segment_placement= ---> <--- > > readgroup = comp4715_c0_seq1._library_2 > data = > /home/ABTLUS/maria.villa/RNASeq_Pseudozyma/read_by_contig/comp4715_c0_seq1_Xilano_1_AGTCAA_merge_R1_001.fastq > /home/ABTLUS/maria.villa/RNASeq_Pseudozyma/read_by_contig/comp4715_c0_seq1_Xilano_1_AGTCAA_merge_R2_001.fastq > technology = solexa > strain = pseudozyma > segment_placement= ---> <--- > > readgroup = comp4715_c0_seq1._library_3 > data = > /home/ABTLUS/maria.villa/RNASeq_Pseudozyma/read_by_contig/comp4715_c0_seq1_Xilose_1_GGCTAC_merge_R1_001.fastq > /home/ABTLUS/maria.villa/RNASeq_Pseudozyma/read_by_contig/comp4715_c0_seq1_Xilose_1_GGCTAC_merge_R2_001.fastq > technology = solexa > strain = pseudozyma > segment_placement= ---> <--- > > -- > Camila M. > -- Camila M.