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Mapping-Assisted Targeted-Assembly for Metagenomics
When running matam_v1.3.0 with a depleted version of SILVA database, an error occured: ```bash 2017-10-16 13:26:24,198 - DEBUG - CMD: cat /workdir/lcouderc/data_matam/16S_rRNA/simulated_dataset/50x/matam/matam_v1.3.0_S128_SSURef_NR95_depleted_cov_50/genomes_complets.art_HS25_pe_1 01bp_50x.sortmerna_vs_SILVA_128_SSURef_NR95_b10_m10.scr_filt_geo_90pct.cov_filt_50.ovgb_i100_o50.cpts_N1_E1.read_metanode_component_taxo.tab | sort -T /workdir/lcouderc/data_matam/16S_r RNA/simulated_dataset/50x/matam/matam_v1.3.0_S128_SSURef_NR95_depleted_cov_50 -S 10000M...
Change how reads pairs are sorted through by reading SAM file reference by reference and using a positions window gliding on each reference. One major problem: How to store read...
- [ ] In debug mode, there is too much verbosity on the contigs assembly step. Restrict the logs to the assembly of the first component and the last one...
Right now we do not use the scaffolding step since we treat all reads as single reads. Using paired-end reads could allow us to use the scaffolding step from SGA...
Right now, all reads are treated as single reads. Some steps could benefit from using paired-end information (contigs assembly with SGA, MATAM scaffolding, ...). So we could still accept the...
Paired-end reads could be used to help us chose between compatible contigs that are mapping on the same reference, thus allowing us to discriminate between 2 close species mapping on...
Hi, Any chance of producing the results, i.e. abundance and taxonomy assignment, in BIOM format?
SortMeRNA v2.1b now support them, so we also could in the future.
The read_fasta_file_handle function is duplicated in many locations: ```text scripts/compute_assembly_stats.py scripts/compute_lca_from_tab.py scripts/compute_pairwise_distance_matrix.py scripts/compute_ref_coverage_histogram.py scripts/exonerate_to_sam.py scripts/extract_taxo_from_fasta.py scripts/fasta_clean_name.py scripts/fasta_get_lengths.py scripts/fasta_length_filter.py scripts/fasta_name_filter.py scripts/filter_sam_by_coverage.py scripts/filter_sam_by_pid.py scripts/get_HMP_OTU_psn.py scripts/matam_assembly.py scripts/remove_redundant_sequences.py scripts/replace_Ns_by_As.py scripts/replace_Ns_by_rand_nu.py scripts/sort_fasta_by_length.py ``` The issue...
When running index_default_ssu_rrna_db.py before building MATAM, SortMeRNA indexdb_rna executable is not found but indexing script terminates with no error... $ ./index_default_ssu_rrna_db.py 2017-01-30 11:26:01,604 - INFO - -- Get compressed archive...