--- /dev/null	Thu Jan 01 00:00:00 1970 +0000
+++ b/PsiCLASS-1.0.2/samtools-0.1.19/bcftools/bcf.tex	Fri Mar 26 16:52:45 2021 +0000
@@ -0,0 +1,77 @@
+\documentclass[10pt,pdftex]{article}
+\usepackage{color}
+\definecolor{gray}{rgb}{0.7,0.7,0.7}
+
+\setlength{\topmargin}{0.0cm}
+\setlength{\textheight}{21.5cm}
+\setlength{\oddsidemargin}{0cm} 
+\setlength{\textwidth}{16.5cm}
+\setlength{\columnsep}{0.6cm}
+
+\begin{document}
+
+\begin{center}
+\begin{tabular}{|l|l|l|l|l|}
+\hline
+\multicolumn{2}{|c|}{\bf Field} & \multicolumn{1}{c|}{\bf Descrption} & \multicolumn{1}{c|}{\bf Type} & \multicolumn{1}{c|}{\bf Value} \\\hline\hline
+\multicolumn{2}{|l|}{\sf magic} & Magic string & {\tt char[4]} & {\tt BCF\char92 4} \\\hline
+\multicolumn{2}{|l|}{\sf l\_seqnm} & Length of concatenated sequence names & {\tt int32\_t} & \\\hline
+\multicolumn{2}{|l|}{\sf seqnm} & Concatenated names, {\tt NULL} padded & {\tt char[{\sf l\_seqnm}]} & \\\hline
+\multicolumn{2}{|l|}{\sf l\_smpl} & Length of concatenated sample names & {\tt int32\_t} & \\\hline
+\multicolumn{2}{|l|}{\sf smpl} & Concatenated sample names & {\tt char[{\sf l\_smpl}]} & \\\hline
+\multicolumn{2}{|l|}{\sf l\_meta} & Length of the meta text (double-hash lines)& {\tt int32\_t} & \\\hline
+\multicolumn{2}{|l|}{\sf meta} & Meta text, {\tt NULL} terminated & {\tt char[{\sf l\_meta}]} & \\\hline
+\multicolumn{5}{|c|}{\it \color{gray}{List of records until the end of the file}}\\\cline{2-5}
+& {\sf seq\_id} & Reference sequence ID & {\tt int32\_t} & \\\cline{2-5}
+& {\sf pos} & Position & {\tt int32\_t} & \\\cline{2-5}
+& {\sf qual} & Variant quality & {\tt float} & \\\cline{2-5}
+& {\sf l\_str} & Length of {\sf str} & {\tt int32\_t} & \\\cline{2-5}
+& {\sf str} & {\tt ID+REF+ALT+FILTER+INFO+FORMAT}, {\tt NULL} padded & {\tt char[{\sf l\_str}]} &\\\cline{2-5}
+& \multicolumn{4}{c|}{Blocks of data; \#blocks and formats defined by {\tt FORMAT} (table below)}\\
+\hline
+\end{tabular}
+\end{center}
+
+\begin{center}
+\begin{tabular}{clp{9cm}}
+\hline
+\multicolumn{1}{l}{\bf Field} & \multicolumn{1}{l}{\bf Type} & \multicolumn{1}{l}{\bf Description} \\\hline
+{\tt DP} & {\tt uint16\_t[n]} & Read depth \\
+{\tt GL} & {\tt float[n*G]} & Log10 likelihood of data; $G=\frac{A(A+1)}{2}$, $A=\#\{alleles\}$\\
+{\tt GT} & {\tt uint8\_t[n]} & {\tt missing\char60\char60 7 | phased\char60\char60 6 | allele1\char60\char60 3 | allele2} \\
+{\tt \_GT} & {\tt uint8\_t+uint8\_t[n*P]} & {Generic GT; the first int equals the max ploidy $P$. If the highest bit is set,
+	the allele is not present (e.g. due to different ploidy between samples).} \\
+{\tt GQ} & {\tt uint8\_t[n]} & {Genotype quality}\\
+{\tt HQ} & {\tt uint8\_t[n*2]} & {Haplotype quality}\\
+{\tt \_HQ} & {\tt uint8\_t+uint8\_t[n*P]} & {Generic HQ}\\
+{\tt IBD} & {\tt uint32\_t[n*2]} & {IBD}\\
+{\tt \_IBD} & {\tt uint8\_t+uint32\_t[n*P]} & {Generic IBD}\\
+{\tt PL} & {\tt uint8\_t[n*G]} & {Phred-scaled likelihood of data}\\
+{\tt PS} & {\tt uint32\_t[n]} & {Phase set}\\
+%{\tt SP} & {\tt uint8\_t[n]} & {Strand bias P-value (bcftools only)}\\
+\emph{Integer} & {\tt int32\_t[n*X]} & {Fix-sized custom Integer; $X$ defined in the header}\\
+\emph{Numeric} & {\tt double[n*X]} & {Fix-sized custom Numeric}\\
+\emph{String} & {\tt uint32\_t+char*} & {\tt NULL} padded concat. strings (int equals to the length) \\
+\hline
+\end{tabular}
+\end{center}
+
+\begin{itemize}
+\item A BCF file is in the {\tt BGZF} format.
+\item All multi-byte numbers are little-endian.
+\item In a string, a missing value `.' is an empty C string ``{\tt
+    \char92 0}'' (not ``{\tt .\char92 0}'')
+\item For {\tt GL} and {\tt PL}, likelihoods of genotypes appear in the
+  order of alleles in {\tt REF} and then {\tt ALT}. For example, if {\tt
+    REF=C}, {\tt ALT=T,A}, likelihoods appear in the order of {\tt
+    CC,CT,TT,CA,TA,AA} (NB: the ordering is different from the one in the original
+	BCF proposal).
+\item Predefined {\tt FORMAT} fields can be missing from VCF headers, but custom {\tt FORMAT} fields
+	are required to be explicitly defined in the headers.
+\item A {\tt FORMAT} field with its name starting with `{\tt \_}' is specific to BCF only.
+	It gives an alternative binary representation of the corresponding VCF field, in case
+	the default representation is unable to keep the genotype information,
+	for example, when the ploidy is not 2 or there are more than 8 alleles.
+\end{itemize}
+
+\end{document}