VCF Files: Store all your Variants, and MoreHave you ever wondered how scientists and bioinformaticians store, access, and organize the genetic variants they discover in each sample? This is the purpose of the Variant Call Format (VCF). To tie in with what we've already discussed in previous p...1ZJul 22, 2023 · 6 min readtaniguti.hashnode.dev
Exploring Spider Genomes: Assessing Assembly CompletenessWhen I was a child, my parents gifted me a fascinating magazine series dedicated to the discovery of Earth's "mini monsters" – tiny creatures that inhabit our planet. Little did I know that today dozens of spider genomes would be available, and scien...Jun 28, 2023 · 6 min readtaniguti.hashnode.dev
BAM Files: When Sequence Reads Match with ReferencesNo matter if you obtained your sequence from Illumina, Nanopore or Sanger, it's always possible to align their nucleotide bases against a reference sequence. It is common to call this reference sequence a "Reference Genome" if it represents the whole...Jun 8, 2023 · 8 min readtaniguti.hashnode.dev
Communication Dichotomies: balancing your toneAt the start of this year, I read a book named "Effective Remote Work". This resource discusses the rise of remote work due to the pandemic, the key challenges of this transition, and provides practical tips for maintaining or even increasing product...Jun 5, 2023 · 8 min readtaniguti.hashnode.dev
FASTQ Files: Everywhere You Look in BioinformaticsI dare say that every bioinformatician working with genomics has encountered FASTQ files. Usually, after ordering DNA sequencing, we receive these files filled with tons of reads. But what exactly are these files? Where do they come from? And most im...May 27, 2023 · 8 min readtaniguti.hashnode.dev