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I'm new to bioinformatics analysis and have two basic questions:
- If I use the recommended reference genome file GCA_000001405.15_GRCh38_no_alt_analysis_set.fna.gz, how should I choose the corresponding reference genome annotation file?
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Must I download the matched GCF file from NCBI (GCA_000001405.15 → GCF_000001405.26),
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or can I use the latest annotation files from GENCODE, Ensembl, or UCSC instead?
- For the same samples, we also performed short-read RNA-seq. Is the GCA_000001405.15_GRCh38_no_alt_analysis_set.fna.gz reference genome suitable for RNA-seq data analysis?
Thank you for your guidance!
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