Happy...unhappy...happy...unhappy...
and this inconsistency may keep up going for a long time.
In order to get rid of this cycle and to stay mentally healthy then better to go with data [Survival kit#1].
:P
Taking the attendance in the genome may be disappointing for some guys at least for the time being. They are there but not really :)
Info for non-science readers: Exon: Coding sequence of DNA present in mature messenger RNA. Intron: Non-coding sequence of DNA removed from mature messenger RNA prior to translation [GeneReviews [Internet], Illustrated glossary]
The term "sequence analysis" in biology implies subjecting a DNA or peptide sequence to sequence alignment, sequence databases, repeated sequence searches, or other bioinformatics methods on a computer. [Wikipedia]
Info for non-science readers: SNPs are one of the most common types of genetic variation. A SNP is a single base pair mutation at a specific locus, usually consisting of two alleles (where the rare allele frequency is >1%). SNPs are found to be the etiology of many human diseases. SNP genotyping is the measurement of genetic variations of single nucleotide polymorphisms (SNPs) between members of a species. It is a form of genotyping, the measurement of the genetic variation more generally. Exome sequencing is an efficient strategy to selectively sequence the coding regions of the human genome to identify novel genes associated with rare and common disorders. RNA-seqis a revolutionary tool for transcriptomics refers to the use of high-throughput sequencing technologies to sequence cDNA in order to get information about a sample's RNA content, a technique that is quickly becoming invaluable in the study of diseases like cancer.