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Update doc to simplify case-study pointers
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README.md

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@@ -16,9 +16,8 @@ DeepVariant supports germline variant-calling in diploid organisms.
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* NGS (Illumina or Element) data for either a
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[whole genome](docs/deepvariant-case-study.md) or
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[whole exome](docs/deepvariant-exome-case-study.md).
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* PacBio HiFi data, see the
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* PacBio HiFi data
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[PacBio case study](docs/deepvariant-pacbio-model-case-study.md).
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* PacBio [Iso-Seq/MAS-Seq case study](docs/deepvariant-masseq-case-study.md).
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* Oxford Nanopore R10.4.1
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[Simplex case study](docs/deepvariant-ont-r104-simplex-case-study.md),
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[Duplex case study](docs/deepvariant-ont-r104-duplex-case-study.md).
@@ -27,7 +26,9 @@ DeepVariant supports germline variant-calling in diploid organisms.
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[G400 case study](docs/deepvariant-complete-g400-case-study.md).
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* Pangenome-mapping-based case-study:
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[vg case study](docs/deepvariant-vg-case-study.md).
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* Illumina [RNA-seq Case Study](docs/deepvariant-rnaseq-case-study.md).
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* RNA data for
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[PacBio Iso-Seq/MAS-Seq case study](docs/deepvariant-masseq-case-study.md)
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and [Illumina RNA-seq Case Study](docs/deepvariant-rnaseq-case-study.md).
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* Hybrid PacBio HiFi + Illumina WGS, see the
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[hybrid case study](docs/deepvariant-hybrid-case-study.md).
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