# White Papers

White papers found in this section provide detailed information about Partek Genomics Suite functionality.

* [Allele Intensity Import](https://help.partek.illumina.com/partek-genomics-suite/white-papers/allele-intensity-import)
* [Allele-Specific Copy Number](https://help.partek.illumina.com/partek-genomics-suite/white-papers/allele-specific-copy-number)
* [Calculating Genotype Likelihoods](https://help.partek.illumina.com/partek-genomics-suite/white-papers/calculating-genotype-likelihoods)
* [ChIP-Seq Peak Detection](https://help.partek.illumina.com/partek-genomics-suite/white-papers/chip-seq-peak-detection)
* [Detect Regions of Significance](https://help.partek.illumina.com/partek-genomics-suite/white-papers/detect-regions-of-significance)
* [Genomic Segmentation](https://help.partek.illumina.com/partek-genomics-suite/white-papers/genomic-segmentation)
* [Loss of Heterozygosity Analysis](https://help.partek.illumina.com/partek-genomics-suite/white-papers/loss-of-heterozygosity-analysis)
* [Motif Discovery Methods](https://help.partek.illumina.com/partek-genomics-suite/white-papers/motif-discovery-methods)
* [Partek Genomics Suite Security](https://help.partek.illumina.com/partek-genomics-suite/white-papers/partek-genomics-suite-security)
* [Reads in RNA-Seq](https://help.partek.illumina.com/partek-genomics-suite/white-papers/reads-in-rna-seq)
* [RNA-Seq Methods](https://help.partek.illumina.com/partek-genomics-suite/white-papers/rna-seq-methods)
* [Unpaired Copy Number Estimation](https://help.partek.illumina.com/partek-genomics-suite/white-papers/unpaired-copy-number-estimation)

## Additional Assistance

If you need additional assistance, please visit [our support page](http://www.partek.com/support) to submit a help ticket or find phone numbers for regional support.