Sentence examples for many analyses including from inspiring English sources

Many analyses, including a new study published in the British medical journal The Lancet this week, have found that mammograms are lifesaving.

Many analyses, including taxonomic delineation, characterization of demographic events, estimates of inbreeding or relatedness, can be successfully conducted in the absence of a genome reference.

Structural equation modelling is an enormously flexible technique – it is possible to use a structural equation modelling approach to carry out direct equivalents of many analyses, including (but not limited to): ANOVA, correlation, ANCOVA, multiple regression, multivariate analysis of variance, and multivariate regression.

Most concerning, instead of basing the calculation of QALYs consistently on utilities that were obtained in a single European neighbor population as response to a lack of primary German data, many analyses included in our review mixed multiple sources.

The Bowdoin study is one of many such analyses, including a book out this month: Why Are Professors Liberal and Why Do Conservatives Care?

Namely, in many survival analyses including several clinicopathological factors, stage is an independent prognostic factor.

As we are using the same set of genes that are present in many other analyses (including some of those used to establish the putative supergroups), there is some circularity in the comparison between our and previously published analyses.

Additionally, a well annotated reference transcriptome can be used for many downstream analyses, including RNA-seq approaches to tissue- or genome-wide gene expression profiling, where it serves as a map for quantifying transcript abundance from short sequencing reads [ 9].

A variety of network structures and network "motifs" (e.g., feedback loops, feedforward loops, and regulatory changes) are over- or underrepresented in ChIP-chip networks (e.g. Lee et al. 2002 and many subsequent analyses including Luscombe et al. 2004 ).

We observe that a tally data structure, i.e. the table of counts of nucleotides × samples × strands × genomic positions, provides a reasonable intermediate level of abstraction for many genomics analyses, including single nucleotide variant (SNV) and InDel calling, copy-number estimation and mutation spectrum analysis.

And yet multiple sequence alignments (MSAs) are a fundamental prerequisite for many downstream comparative analyses, including phylogenetic inference.