What data have been complied in the Human Protein Atlas? https://www.proteinatlas.org/about  A.The Human Protein Atlas was created by integrating different omics technologies such as antibody-based imaging, proteomic analysis by mass spectrometry, transcriptomics and systems biology. B.The Human Protein Atlas was established by examining the distribution of proteins in a diseased tissue and inferring where the protein localize in a healthy tissue. C.The Human Protein Atlas was created by creating a list of all know proteins in alphabetical order. D.The Human Protein Atlas was created immunoblot analysis of proteins in different tissues.

Briefly describe the method of chromatin immunoprecipitation sequencing (ChIP-Seq). How is it used to determine nucleosome positions within a genome?

Based on the NCBI blast below Are there any pathogenic missense mutations in the human gene FGFR3? Also do they have any identical amino acids to prove a mouse is the best model to test the fgfr3 gene?

In Northern blot analysis, mRNA samples from tissues are bound to a labeled DNA probe that is complementary to the mRNA, and run on a gel to be visualized. The protein tropomyosin is known to be present in both brain and liver.  When brain and liver tissue were assayed for the presence of tropomyosin mature mRNA, bands of two different sizes were seen. Tropomyosin gene diagram (3000 bp total): Shown in attatched image If the band on the Northern blot for mRNA isolated from liver tissue is 2580 bp, whereas from brain tissue the band is 2250 bp, what is most likely? a)The two mRNAs are made from different tropomyosin DNA sequences. b)Exon 2 is alternatively spliced out of the brain mRNA. c)Introns 1 and 2 are spliced out of the brain transcript but not the liver transcript. d)Exons 1 and 3 are spliced out of the brain transcript but not the liver transcript. e)Exon 2 is alternatively spliced out of the liver mRNA.