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Exact(4)
Probes mapping to common variant SNPs or non-unique mappings were removed from the analysis, leaving 330,557 probes for the downstream analysis [ 115].
The non-unique mappings were removed.
Thus, 17% the reads' mappings were removed by our filter.
All data and scripts are available online [ 58].> -wrap-foot> Genes corresponding with haplotype variants, unmapped contig regions and low confidence RNA-seq mappings were removed, resulting in a set of 38,041 genes for analysis.
Similar(56)
Reads with more than one mapping location were removed to avoid bias caused by multi-mapping reads.
All reads with ambiguous paired mappings and all redundant pairs were removed.
A further nine UMLS mappings pointed to non-existent FMA URI's and were removed.
Any markers which overlapped another marker were removed, as were markers with non-unique mappings.
Multiple transcripts or isoforms were removed by considering only the most 5′-located TSS for each unique Ensembl gene identifier, resulting in a set of 11,806 genes with unambiguous mappings.
Candidates involving alignments marked as multi-mapping can be removed at the filtering stage, if desired (see below).
If both reads of a pair were displaced by new mappings, then that read pair was removed from the extension/linkage dataset.
Related(20)
correlations were removed
mappings were resolved
predictions were removed
connections were removed
mappings were retrieved
assignments were removed
mappings were observed
allocation were removed
mappings were carried
mappings were considered
mappings were derived
mappings were stated
mappings were evaluated
mappings were designed
mappings were compared
mappings were studied
mappings were proposed
mappings were converged
mappings were introduced
mappings were counted
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