Three examples show why in the sequence case so direct formula is rather impossible.
Structural specifications of the distillation columns were the same for the proposed model and base direct sequence case.
If however we include SLAs, even on sequence case, we already have an NP-hard problem to solve.
In the first case the characteristic is expressed in terms of the generating Orlicz function only, but in the sequence case the formula is not so direct.
Analogous results for Orlicz-Lorentz sequence spaces were presented in [14], but the techniques of the proofs in the function case are different (in some parts completely different) than in the sequence case.
One would not want to simply discard all sequenced cases when counting alleles for an association test.
Sequencing cases would find many variants not found in controls, but sequencing controls would likely find as many variants not found in cases, and neither disparity would have anything to do with the disease.
We also found an intronic insertion IVS17-50insatat exon 18 in all sequenced cases.
For 368 (of 373) sequenced cases, detailed clinical data were available for statistical analysis.
In most of the recent whole-genome sequencing cases, whole-genome sequences are generated using next-generation sequencing (NGS).
