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Target validation and protein measures were done for selected genes to further confirm functional relevance.
We focused on the seven novel genes to further investigate why they escaped computational prediction.
We performed gene function enrichment analysis on these genes to further categorize them into biological functions.
Future investigations can now target identified genes to further characterize their specific actions in the networks regulating follicle assembly.
We applied IPA to the list of differential genes to further explore the biological significance of the expression data.
Then we performed the receiver-operator characteristic (ROC) analysis for the connected genes to further verify their connections.
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Therefore, we used this gene to further study the role of Sp1 in its transcription.
Given that fibronectin's alternative splicing variants are well described and have been extensively studied [35], [36], [37], we decided to use this gene to further characterize the role of HDACs in alternative splicing.
Therefore, HSD4 provides an interesting candidate gene to further study processes directly linked to competition.
We used a synthetic Gaussia princeps luciferase gene to further assess the binding of GvpC fusion proteins to gas vesicles.
We select a single probe for each gene to further avoid biases in gene set tests from using multiple probes for a single gene.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com