In with two points, fiting a linear model is straightforward (whatever the technique considered). Here, we’re simply considering the straight line that passes through the other two points. And since we have the straight line (without the minimal calculation of minimizing the sum of squared ...
sigmaSquared - this is the variance of the phenotype, in this example rand_qt is the phenotype. nSamples - number of samples that went into the analysis variants - an array of variant objects, each containing a score statistic, p-value, and alt allele frequency groups - an array of ...
By default selscan calculates homozygosity values using binomial coefficents. Hapbin uses the sum of the squared haplotype frequencies which can also be used by selscan using the --alt flag. When the --alt flag is used with selscan the two approaches should be comparable. ...
python.ops import math_ops from tensorflow.python.ops import nn_ops rnn_cell = tf.nn.rnn_cell seq2seq = tf.nn.seq2seq def complex_mul_real( c, r ): return tf.complex(tf.real(c)*r, tf.imag(c)*r) def refl_c(in_, normal_): normal_rk2 = tf.expand_dims( normal_, 1 ) ...
sigmaSquared - this is the variance of the phenotype, in this example rand_qt is the phenotype. nSamples - number of samples that went into the analysis variants - an array of variant objects, each containing a score statistic, p-value, and alt allele frequency groups - an array of ...
sigmaSquared - this is the variance of the phenotype, in this example rand_qt is the phenotype. nSamples - number of samples that went into the analysis variants - an array of variant objects, each containing a score statistic, p-value, and alt allele frequency groups - an array of ...