Entering edit mode
4.6 years ago
zhangdengwei
▴
210
Hi all,
I am using metaphlan 3
to profile the microbial composition, and I found the difference between two parameters, specifically, the following parameters:
-t ANALYSIS TYPE Type of analysis to perform:
* rel_ab: profiling a metagenomes in terms of relative abundances
* rel_ab_w_read_stats: profiling a metagenomes in terms of relative abundances and estimate the number of reads coming from each clade.
* reads_map: mapping from reads to clades (only reads hitting a marker)
* clade_profiles: normalized marker counts for clades with at least a non-null marker
* marker_ab_table: normalized marker counts (only when > 0.0 and normalized by metagenome size if --nreads is specified)
* marker_counts: non-normalized marker counts [use with extreme caution]
* marker_pres_table: list of markers present in the sample (threshold at 1.0 if not differently specified with --pres_th
[default 'rel_ab']
the default is rel_ab
, when using this parameter, the item relative abundances
is proportion in output, the abundance in each level can sum to 100. However, when using -t rel_ab_w_read_stats
, the abundance in each level cannot sum to 100, so what's meaning of relative abundance
in this case? Can I directly compare their abundance between different groups?
Thanks in advance!
Did you figure it out? I am also stuck at this step. Can you please help me out?
The output from
rel_ab_w_read_stats
should be reads count. You can convert it into proportion manually, which is akin to the output ofrel_ab
.But when you convert it to relative abundance using
-t rel_ab_w_read_stats
, it is not same as of the abundance output fromrel_ab
Thanks
But when you convert it to relative abundance using
-t rel_ab_w_read_stats
, it is not same as of the abundance output fromrel_ab
Thanks
Could it be, that
-t rel_ab_w_read_stats
havn't been normalized to clade-marker coverage? But that would be in contrast to the name relative abundances with read stats.